{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T14:42:52Z","timestamp":1786977772281,"version":"build-2736575974"},"reference-count":46,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2018,8,22]],"date-time":"2018-08-22T00:00:00Z","timestamp":1534896000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"},{"start":{"date-parts":[[2018,8,22]],"date-time":"2018-08-22T00:00:00Z","timestamp":1534896000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100000925","name":"National Health and Medical Research Council","doi-asserted-by":"publisher","award":["334314"],"award-info":[{"award-number":["334314"]}],"id":[{"id":"10.13039\/501100000925","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100000925","name":"National Health and Medical Research Council","doi-asserted-by":"publisher","award":["546517"],"award-info":[{"award-number":["546517"]}],"id":[{"id":"10.13039\/501100000925","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Human Mutation"],"published-print":{"date-parts":[[2018,12]]},"DOI":"10.1002\/humu.23603","type":"journal-article","created":{"date-parts":[[2018,8,2]],"date-time":"2018-08-02T12:46:12Z","timestamp":1533213972000},"page":"1861-1874","source":"Crossref","is-referenced-by-count":19,"title":["Mutant NR5A1\/SF-1 in patients with disorders of sex development shows defective activation of the\n                    <i>SOX9<\/i>\n                    TESCO enhancer"],"prefix":"10.1155","volume":"39","author":[{"given":"Rajini","family":"Sreenivasan","sequence":"first","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"},{"name":"Department of Anatomy and Neuroscience; University of Melbourne; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Louisa","family":"Ludbrook","sequence":"additional","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"},{"name":"Department of Biochemistry and Molecular Biology; Monash University; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brett","family":"Fisher","sequence":"additional","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"},{"name":"Department of Biochemistry and Molecular Biology; Monash University; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Faustine","family":"Declosmenil","sequence":"additional","affiliation":[{"name":"Institut de G\u00e9n\u00e9tique Humaine; Montpellier France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kevin C.","family":"Knower","sequence":"additional","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brittany","family":"Croft","sequence":"additional","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"},{"name":"Department of Molecular Translational Science, Monash University; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anthony D.","family":"Bird","sequence":"additional","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Janelle","family":"Ryan","sequence":"additional","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anu","family":"Bashamboo","sequence":"additional","affiliation":[{"name":"Institut Pasteur; Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew H.","family":"Sinclair","sequence":"additional","affiliation":[{"name":"Murdoch Children's Research Institute, Royal Children's Hospital and Department of Paediatrics; The University of Melbourne; Melbourne Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter","family":"Koopman","sequence":"additional","affiliation":[{"name":"Institute for Molecular Bioscience; The University of Queensland; Brisbane Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ken","family":"McElreavey","sequence":"additional","affiliation":[{"name":"Institut Pasteur; Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Francis","family":"Poulat","sequence":"additional","affiliation":[{"name":"Department of Molecular Translational Science, Monash University; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2405-1262","authenticated-orcid":false,"given":"Vincent R.","family":"Harley","sequence":"additional","affiliation":[{"name":"Hudson Institute of Medical Research; Victoria Australia"},{"name":"Department of Biochemistry and Molecular Biology; Monash University; Victoria Australia"},{"name":"Department of Anatomy and Developmental Biology; Monash University; Victoria Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2018,8,22]]},"reference":[{"issue":"2","key":"10.1002\/humu.23603-BIB0001|humu23603-cit-0001","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1038\/9629","article-title":"A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans","volume":"22","author":"Achermann","year":"1999","journal-title":"Nature Genetics"},{"issue":"4","key":"10.1002\/humu.23603-BIB0002|humu23603-cit-0002","doi-asserted-by":"crossref","first-page":"1829","DOI":"10.1210\/jcem.87.4.8376","article-title":"Gonadal determination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner","volume":"87","author":"Achermann","year":"2002","journal-title":"Journal of Clinical Endocrinology and Metabolism"},{"issue":"10","key":"10.1002\/humu.23603-BIB0003|humu23603-cit-0003","doi-asserted-by":"crossref","first-page":"e24117","DOI":"10.1371\/journal.pone.0024117","article-title":"Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias","volume":"6","author":"Allali","year":"2011","journal-title":"Plos One"},{"issue":"4","key":"10.1002\/humu.23603-BIB0004|humu23603-cit-0004","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1016\/j.ajhg.2010.09.009","article-title":"Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1","volume":"87","author":"Bashamboo","year":"2010","journal-title":"American Journal of Human Genetics"},{"key":"10.1002\/humu.23603-BIB0048|humu23603-cit-0048","doi-asserted-by":"crossref","first-page":"825","DOI":"10.1136\/jmedgenet-2011-100255","article-title":"Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development","volume":"48","author":"Benko","year":"2011","journal-title":"Journal of Medical Genetics"},{"issue":"7","key":"10.1002\/humu.23603-BIB0005|humu23603-cit-0005","doi-asserted-by":"crossref","first-page":"E1294","DOI":"10.1210\/jc.2011-3169","article-title":"Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individuals","volume":"97","author":"Camats","year":"2012","journal-title":"Journal of Clinical Endocrinology and Metabolism"},{"issue":"4","key":"10.1002\/humu.23603-BIB0006|humu23603-cit-0006","doi-asserted-by":"crossref","first-page":"1767","DOI":"10.1210\/jc.2003-031240","article-title":"A microdeletion in the ligand binding domain of human steroidogenic factor 1 causes XY sex reversal without adrenal insufficiency","volume":"89","author":"Correa","year":"2004","journal-title":"Journal of Clinical Endocrinology and Metabolism"},{"key":"10.1002\/humu.23603-BIB0007|humu23603-cit-0007","unstructured":"DeLano , W. L. 2010 New York, NY Schr\u00f6dinger, LLC"},{"issue":"1","key":"10.1002\/humu.23603-BIB0008|humu23603-cit-0008","doi-asserted-by":"crossref","first-page":"114","DOI":"10.1002\/humu.23353","article-title":"Functional characterization of five NR5A1 gene mutations found in patients with 46,XY disorders of sex development","volume":"39","author":"Fabbri-Scallet","year":"2018","journal-title":"Human Mutation"},{"issue":"1-2","key":"10.1002\/humu.23603-BIB0009|humu23603-cit-0009","doi-asserted-by":"crossref","first-page":"198","DOI":"10.1016\/j.mce.2010.11.006","article-title":"Steroidogenic factor-1 (SF-1, NR5A1) and human disease","volume":"336","author":"Ferraz-de-Souza","year":"2011","journal-title":"Molecular and Cellular Endocrinology"},{"issue":"4","key":"10.1002\/humu.23603-BIB0010|humu23603-cit-0010","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1111\/j.1442-200X.1996.tb03515.x","article-title":"Mutations in SOX9 cause both autosomal sex reversal and campomelic dysplasia","volume":"38","author":"Foster","year":"1996","journal-title":"Acta Paediatrica Japonica"},{"issue":"6","key":"10.1002\/humu.23603-BIB0011|humu23603-cit-0011","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1159\/000320142","article-title":"Mutations of the SRY-responsive enhancer of SOX9 are uncommon in XY gonadal dysgenesis","volume":"4","author":"Georg","year":"2010","journal-title":"Sexual Development"},{"issue":"1","key":"10.1002\/humu.23603-BIB0012|humu23603-cit-0012","doi-asserted-by":"crossref","first-page":"e1006520","DOI":"10.1371\/journal.pgen.1006520","article-title":"Normal levels of Sox9 expression in the developing mouse testis depend on the TES\/TESCO enhancer, but this does not act alone","volume":"13","author":"Gonen","year":"2017","journal-title":"PLoS Genetics"},{"issue":"1-2","key":"10.1002\/humu.23603-BIB0013|humu23603-cit-0013","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1016\/S0925-4773(99)00123-9","article-title":"Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination","volume":"87","author":"Hanley","year":"1999","journal-title":"Mechanisms of Development"},{"issue":"41","key":"10.1002\/humu.23603-BIB0014|humu23603-cit-0014","doi-asserted-by":"crossref","first-page":"31708","DOI":"10.1074\/jbc.M002892200","article-title":"A naturally occurring steroidogenic factor-1 mutation exhibits differential binding and activation of target genes","volume":"275","author":"Ito","year":"2000","journal-title":"Journal of Biological Chemistry"},{"issue":"2","key":"10.1002\/humu.23603-BIB0015|humu23603-cit-0015","doi-asserted-by":"crossref","first-page":"290","DOI":"10.1210\/mend.12.2.0059","article-title":"Steroidogenic factor-1 contains a carboxy-terminal transcriptional activation domain that interacts with steroid receptor coactivator-1","volume":"12","author":"Ito","year":"1998","journal-title":"Molecular Endocrinology"},{"issue":"4","key":"10.1002\/humu.23603-BIB0016|humu23603-cit-0016","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1136\/jmedgenet-2014-102864","article-title":"Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development","volume":"52","author":"Kim","year":"2015","journal-title":"Journal of Medical Genetics"},{"issue":"3","key":"10.1002\/humu.23603-BIB0017|humu23603-cit-0017","doi-asserted-by":"crossref","first-page":"e17751","DOI":"10.1371\/journal.pone.0017751","article-title":"Failure of SOX9 Regulation in 46,XY Disorders of Sex Development with SRY, SOX9 and SF1 Mutations","volume":"6","author":"Knower","year":"2011","journal-title":"PLoS One"},{"issue":"1","key":"10.1002\/humu.23603-BIB0018|humu23603-cit-0018","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1002\/humu.20588","article-title":"Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency","volume":"29","author":"Kohler","year":"2008","journal-title":"Human Mutation"},{"issue":"3","key":"10.1002\/humu.23603-BIB0019|humu23603-cit-0019","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1016\/j.cell.2005.01.024","article-title":"Structural analyses reveal phosphatidyl inositols as ligands for the NR5 orphan receptors SF-1 and LRH-1","volume":"120","author":"Krylova","year":"2005","journal-title":"Cell"},{"issue":"8","key":"10.1002\/humu.23603-BIB0020|humu23603-cit-0020","first-page":"1249","article-title":"Steroidogenic factor I, a key regulator of steroidogenic enzyme expression, is the mouse homolog of fushi tarazu-factor I","volume":"6","author":"Lala","year":"1992","journal-title":"Molecular Endocrinology"},{"issue":"4","key":"10.1002\/humu.23603-BIB0021|humu23603-cit-0021","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1016\/j.molcel.2005.02.002","article-title":"Crystallographic identification and functional characterization of phospholipids as ligands for the orphan nuclear receptor steroidogenic factor-1","volume":"17","author":"Li","year":"2005","journal-title":"Molecular Cell"},{"issue":"3","key":"10.1002\/humu.23603-BIB0022|humu23603-cit-0022","doi-asserted-by":"crossref","first-page":"991","DOI":"10.1210\/jc.2006-1672","article-title":"Heterozygous missense mutations in steroidogenic factor 1 (SF1\/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function","volume":"92","author":"Lin","year":"2007","journal-title":"Journal of Clinical Endocrinology and Metabolism"},{"issue":"4","key":"10.1002\/humu.23603-BIB0023|humu23603-cit-0023","doi-asserted-by":"crossref","first-page":"831","DOI":"10.1210\/me.2005-0384","article-title":"Sequence-specific deoxyribonucleic acid (DNA) recognition by steroidogenic factor 1: A helix at the carboxy terminus of the DNA binding domain is necessary for complex stability","volume":"20","author":"Little","year":"2006","journal-title":"Molecular Endocrinology"},{"issue":"4","key":"10.1002\/humu.23603-BIB0024|humu23603-cit-0024","doi-asserted-by":"crossref","first-page":"1948","DOI":"10.1210\/en.2011-1428","article-title":"Excess DAX1 leads to XY ovotesticular disorder of sex development (DSD) in mice by inhibiting steroidogenic factor-1 (SF1) activation of the testis enhancer of SRY-box-9 (Sox9)","volume":"153","author":"Ludbrook","year":"2012","journal-title":"Endocrinology"},{"issue":"4","key":"10.1002\/humu.23603-BIB0025|humu23603-cit-0025","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1016\/0092-8674(94)90211-9","article-title":"A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation","volume":"77","author":"Luo","year":"1994","journal-title":"Cell"},{"issue":"3","key":"10.1002\/humu.23603-BIB0026|humu23603-cit-0026","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1159\/000445983","article-title":"Identification of NR5A1 mutations and possible digenic inheritance in 46,XY gonadal dysgenesis","volume":"10","author":"Mazen","year":"2016","journal-title":"Sexual Development"},{"issue":"25","key":"10.1002\/humu.23603-BIB0027|humu23603-cit-0027","doi-asserted-by":"crossref","first-page":"17913","DOI":"10.1016\/S0021-9258(19)37129-7","article-title":"A common trans-acting factor, Ad4-binding protein, to the promoters of steroidogenic P-450s","volume":"267","author":"Morohashi","year":"1992","journal-title":"Journal of Biological Chemistry"},{"issue":"3","key":"10.1002\/humu.23603-BIB0028|humu23603-cit-0028","doi-asserted-by":"crossref","first-page":"372","DOI":"10.1016\/S1016-8478(23)07353-3","article-title":"EID-1 interacts with orphan nuclear receptor SF-1 and represses its transactivation","volume":"24","author":"Park","year":"2007","journal-title":"Molecules and Cells"},{"key":"10.1002\/humu.23603-BIB0030|humu23603-cit-0030","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1007\/978-1-4419-8002-1_16","article-title":"Phenotypic variation of SF1 gene mutations","volume":"707","author":"Philibert","year":"2011","journal-title":"Advances in Experimental Medicine and Biology"},{"issue":"5","key":"10.1002\/humu.23603-BIB0031|humu23603-cit-0031","doi-asserted-by":"crossref","first-page":"e1785","DOI":"10.1016\/j.fertnstert.2010.11.035","article-title":"Predominant Sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1\/SF-1 mutation transmitted by his unaffected father","volume":"95","author":"Philibert","year":"2011","journal-title":"Fertility and Sterility"},{"issue":"12","key":"10.1002\/humu.23603-BIB0032|humu23603-cit-0032","doi-asserted-by":"crossref","first-page":"3255","DOI":"10.1093\/humrep\/dem278","article-title":"Mutational analysis of steroidogenic factor 1 (NR5A1) in 24 boys with bilateral anorchia: A French collaborative study","volume":"22","author":"Philibert","year":"2007","journal-title":"Human Reproduction"},{"issue":"6","key":"10.1002\/humu.23603-BIB0033|humu23603-cit-0033","doi-asserted-by":"crossref","first-page":"1799","DOI":"10.1210\/jcem.82.6.3967","article-title":"Steroidogenic factor 1 messenger ribonucleic acid expression in steroidogenic and nonsteroidogenic human tissues: Northern blot and in situ hybridization studies","volume":"82","author":"Ramayya","year":"1997","journal-title":"Journal of Clinical Endocrinology and Metabolism"},{"issue":"10","key":"10.1002\/humu.23603-BIB0034|humu23603-cit-0034","doi-asserted-by":"crossref","first-page":"1552","DOI":"10.1210\/mend-5-10-1552","article-title":"A shared promoter element regulates the expression of three steroidogenic enzymes","volume":"5","author":"Rice","year":"1991","journal-title":"Molecular Endocrinology"},{"issue":"1","key":"10.1002\/humu.23603-BIB0035|humu23603-cit-0035","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1002\/humu.23354","article-title":"Functional characterization of novel NR5A1 variants reveals multiple complex roles in disorders of sex development","volume":"39","author":"Robevska","year":"2018","journal-title":"Human Mutation"},{"issue":"24","key":"10.1002\/humu.23603-BIB0036|humu23603-cit-0036","doi-asserted-by":"crossref","first-page":"10939","DOI":"10.1073\/pnas.92.24.10939","article-title":"Mice deficient in the orphan receptor steroidogenic factor 1 lack adrenal glands and gonads but express P450 side-chain-cleavage enzyme in the placenta and have normal embryonic serum levels of corticosteroids","volume":"92","author":"Sadovsky","year":"1995","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"issue":"7197","key":"10.1002\/humu.23603-BIB0037|humu23603-cit-0037","doi-asserted-by":"crossref","first-page":"930","DOI":"10.1038\/nature06944","article-title":"Sex determination involves synergistic action of SRY and SF1 on a specific Sox9 enhancer","volume":"453","author":"Sekido","year":"2008","journal-title":"Nature"},{"key":"10.1002\/humu.23603-BIB0038|humu23603-cit-0038","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1007\/978-1-4419-8002-1_33","article-title":"Inguinal hernia in a phenotypic female infant may reveal a 46XY sex reversal, supported by the identification of a novel SF1 gene mutation","volume":"707","author":"Sinha","year":"2011","journal-title":"Advances in Experimental Medicine and Biology"},{"issue":"8","key":"10.1002\/humu.23603-BIB0039|humu23603-cit-0039","first-page":"1388","article-title":"Transcription factor GATA-4 enhances Mullerian inhibiting substance gene transcription through a direct interaction with the nuclear receptor SF-1","volume":"13","author":"Tremblay","year":"1999","journal-title":"Molecular Endocrinology"},{"issue":"13","key":"10.1002\/humu.23603-BIB0040|humu23603-cit-0040","doi-asserted-by":"crossref","first-page":"3689","DOI":"10.1093\/nar\/19.13.3689","article-title":"Defining the sequence recognized with BmFTZ-F1, a sequence specific DNA binding factor in the silkworm, Bombyx mori, as revealed by direct sequencing of bound oligonucleotides and gel mobility shift competition analysis","volume":"19","author":"Ueda","year":"1991","journal-title":"Nucleic Acids Research"},{"issue":"12","key":"10.1002\/humu.23603-BIB0041|humu23603-cit-0041","doi-asserted-by":"crossref","first-page":"5667","DOI":"10.1128\/MCB.12.12.5667","article-title":"A novel DNA-binding motif abuts the zinc finger domain of insect nuclear hormone receptor FTZ-F1 and mouse embryonal long terminal repeat-binding protein","volume":"12","author":"Ueda","year":"1992","journal-title":"Molecular and Cellular Biology"},{"issue":"3","key":"10.1002\/humu.23603-BIB0042|humu23603-cit-0042","doi-asserted-by":"crossref","first-page":"787","DOI":"10.1016\/j.fertnstert.2005.09.016","article-title":"Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1","volume":"85","author":"Wada","year":"2006","journal-title":"Fertility and Sterility"},{"issue":"4","key":"10.1002\/humu.23603-BIB0043|humu23603-cit-0043","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1507\/endocrj.52.445","article-title":"Association of severe micropenis with Gly146Ala polymorphism in the gene for steroidogenic factor-1","volume":"52","author":"Wada","year":"2005","journal-title":"Endocrine Journal"},{"issue":"21","key":"10.1002\/humu.23603-BIB0044|humu23603-cit-0044","doi-asserted-by":"crossref","first-page":"7505","DOI":"10.1073\/pnas.0409482102","article-title":"The crystal structures of human steroidogenic factor-1 and liver receptor homologue-1","volume":"102","author":"Wang","year":"2005","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"issue":"4","key":"10.1002\/humu.23603-BIB0045|humu23603-cit-0045","doi-asserted-by":"crossref","first-page":"987","DOI":"10.1016\/j.bbrc.2003.10.096","article-title":"Functional characterization of a new human Ad4BP\/SF-1 variation, G146A","volume":"311","author":"WuQiang","year":"2003","journal-title":"Biochemical and Biophysical Research Communications"},{"issue":"5","key":"10.1002\/humu.23603-BIB0046|humu23603-cit-0046","doi-asserted-by":"crossref","first-page":"2071","DOI":"10.1172\/JCI73186","article-title":"Testicular differentiation factor SF-1 is required for human spleen development","volume":"124","author":"Zangen","year":"2014","journal-title":"Journal of Clinical Investigation"}],"container-title":["Human Mutation"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fhumu.23603","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1002\/humu.23603\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,7,8]],"date-time":"2024-07-08T18:11:54Z","timestamp":1720462314000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/humu.23603"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,8,22]]},"references-count":46,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2018,12]]}},"URL":"https:\/\/doi.org\/10.1002\/humu.23603","archive":["Portico"],"relation":{},"ISSN":["1059-7794"],"issn-type":[{"value":"1059-7794","type":"print"}],"subject":[],"published":{"date-parts":[[2018,8,22]]}}}