{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,12]],"date-time":"2026-03-12T09:12:46Z","timestamp":1773306766139,"version":"3.50.1"},"reference-count":49,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2018,12,21]],"date-time":"2018-12-21T00:00:00Z","timestamp":1545350400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"},{"start":{"date-parts":[[2018,12,21]],"date-time":"2018-12-21T00:00:00Z","timestamp":1545350400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001659","name":"Deutsche Forschungsgemeinschaft","doi-asserted-by":"publisher","award":["KU 1240\/6-2"],"award-info":[{"award-number":["KU 1240\/6-2"]}],"id":[{"id":"10.13039\/501100001659","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Science and Engineering Research Board, The Department of Science and Technology, Government of India","award":["SB\/SO\/HS\/005\/2014"],"award-info":[{"award-number":["SB\/SO\/HS\/005\/2014"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Human Mutation"],"published-print":{"date-parts":[[2019,3]]},"DOI":"10.1002\/humu.23693","type":"journal-article","created":{"date-parts":[[2018,11,29]],"date-time":"2018-11-29T09:51:01Z","timestamp":1543485061000},"page":"299-309","source":"Crossref","is-referenced-by-count":65,"title":["The homozygous variant c.797G&gt;A\/p.(Cys266Tyr) in<i>PISD<\/i>is associated with a Spondyloepimetaphyseal dysplasia with large epiphyses and disturbed mitochondrial function"],"prefix":"10.1155","volume":"40","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0139-8239","authenticated-orcid":false,"given":"Katta M.","family":"Girisha","sequence":"first","affiliation":[{"name":"Department of Medical Genetics; Kasturba Medical College; Manipal Academy of Higher Education; Manipal India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Leonie","family":"von Elsner","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics; University Medical Center Hamburg-Eppendorf; Hamburg Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kausthubham","family":"Neethukrishna","sequence":"additional","affiliation":[{"name":"Department of Medical Genetics; Kasturba Medical College; Manipal Academy of Higher Education; Manipal India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mamta","family":"Muranjan","sequence":"additional","affiliation":[{"name":"Department of Clinical Genetics; Seth GS Medical College and KEM Hospital; Mumbai India"},{"name":"Consultant in Clinical Genetics; P.D. Hinduja National Hospital & MRC; Mumbai India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anju","family":"Shukla","sequence":"additional","affiliation":[{"name":"Department of Medical Genetics; Kasturba Medical College; Manipal Academy of Higher Education; Manipal India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gandham SriLakshmi","family":"Bhavani","sequence":"additional","affiliation":[{"name":"Department of Medical Genetics; Kasturba Medical College; Manipal Academy of Higher Education; Manipal India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gen","family":"Nishimura","sequence":"additional","affiliation":[{"name":"Department of Pediatric Imaging; Tokyo Metropolitan Children's Medical Center; Fuchu Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8494-8963","authenticated-orcid":false,"given":"Kerstin","family":"Kutsche","sequence":"additional","affiliation":[{"name":"Institute of Human Genetics; University Medical Center Hamburg-Eppendorf; Hamburg Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Geert","family":"Mortier","sequence":"additional","affiliation":[{"name":"Centre of Medical Genetics; University of Antwerp & University Hospital Antwerp; Antwerp Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2018,12,21]]},"reference":[{"issue":"9","key":"10.1002\/humu.23693-BIB0001|humu23693-cit-0001","doi-asserted-by":"crossref","first-page":"1388\u22121397","DOI":"10.1038\/sj.leu.2402201","article-title":"Proteasome inhibitor-induced apoptosis of B-chronic lymphocytic leukaemia cells involves cytochrome c release and caspase activation, accompanied by formation of an 700 kDa Apaf-1 containing apoptosome complex","volume":"15","author":"Almond","year":"2001","journal-title":"Leukemia"},{"issue":"6","key":"10.1002\/humu.23693-BIB0002|humu23693-cit-0002","doi-asserted-by":"crossref","first-page":"919\u2212929","DOI":"10.1083\/jcb.201308006","article-title":"The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission","volume":"204","author":"Anand","year":"2014","journal-title":"The Journal of Cell Biology"},{"issue":"12","key":"10.1002\/humu.23693-BIB0003|humu23693-cit-0003","first-page":"2869\u22122892","article-title":"Nosology and classification of genetic skeletal disorders: 2015 revision","volume":"167A","author":"Bonafe","year":"2015","journal-title":"American Journal of Medical Genetics Part A"},{"key":"10.1002\/humu.23693-BIB0004|humu23693-cit-0004","doi-asserted-by":"crossref","first-page":"PC28","DOI":"10.1016\/S0021-9258(19)63319-3","article-title":"Enzymatic formation and decarboxylation of phosphatidylserine","volume":"236","author":"Borkenhagen","year":"1961","journal-title":"Journal of Biological Chemistry"},{"issue":"5","key":"10.1002\/humu.23693-BIB0005|humu23693-cit-0005","first-page":"3289\u22123303","article-title":"Glutathione peroxidases","volume":"1830","author":"Brigelius-Flohe","year":"2013","journal-title":"Biochimica et Biophysica Acta"},{"issue":"3","key":"10.1002\/humu.23693-BIB0006|humu23693-cit-0006","doi-asserted-by":"crossref","first-page":"383\u2212396","DOI":"10.1002\/jnr.10493","article-title":"Caspase activation pathways induced by staurosporine and low potassium: Role of caspase-2","volume":"71","author":"Caballero-Benitez","year":"2003","journal-title":"Journal of Neuroscience Research"},{"issue":"9","key":"10.1002\/humu.23693-BIB0007|humu23693-cit-0007","doi-asserted-by":"crossref","first-page":"647\u2212656","DOI":"10.1038\/nrc883","article-title":"The Bcl2 family: Regulators of the cellular life-or-death switch","volume":"2","author":"Cory","year":"2002","journal-title":"Nature Reviews Cancer"},{"issue":"4","key":"10.1002\/humu.23693-BIB0008|humu23693-cit-0008","first-page":"263\u2212269","article-title":"Eight human OPA1 isoforms, long and short: What are they for?","volume":"1859","author":"Del Dotto","year":"2018","journal-title":"Biochimica et Biophysica Acta"},{"issue":"7","key":"10.1002\/humu.23693-BIB0009|humu23693-cit-0009","first-page":"716\u2212725","article-title":"Involvement of a putative substrate binding site in the biogenesis and assembly of phosphatidylserine decarboxylase 1 from Saccharomyces cerevisiae","volume":"1862","author":"Bartolomeo","year":"2017","journal-title":"Biochimica et Biophysica Acta"},{"issue":"4","key":"10.1002\/humu.23693-BIB0010|humu23693-cit-0010","doi-asserted-by":"crossref","first-page":"495","DOI":"10.1080\/01926230701320337","article-title":"Apoptosis: A review of programmed cell death","volume":"35","author":"Elmore","year":"2007","journal-title":"Toxicologic Pathology"},{"issue":"1","key":"10.1002\/humu.23693-BIB0011|humu23693-cit-0011","doi-asserted-by":"crossref","first-page":"3\u221215","DOI":"10.4149\/av_2013_01_3","article-title":"Mortalin-a multipotent chaperone regulating cellular processes ranging from viral infection to neurodegeneration","volume":"57","author":"Flachbartova","year":"2013","journal-title":"Acta Virologica"},{"issue":"3","key":"10.1002\/humu.23693-BIB0012|humu23693-cit-0012","doi-asserted-by":"crossref","first-page":"e1002027","DOI":"10.1371\/journal.pgen.1002027","article-title":"Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia","volume":"7","author":"Glazov","year":"2011","journal-title":"PLoS Genetics"},{"issue":"1","key":"10.1002\/humu.23693-BIB0013|humu23693-cit-0013","doi-asserted-by":"crossref","first-page":"120\u2212129","DOI":"10.1016\/j.ajhg.2009.06.008","article-title":"Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2","volume":"85","author":"Guernsey","year":"2009","journal-title":"The American Journal of Human Genetics"},{"issue":"4","key":"10.1002\/humu.23693-BIB0014|humu23693-cit-0014","doi-asserted-by":"crossref","first-page":"185\u2212194","DOI":"10.1023\/A:1016089607548","article-title":"A decision between life and death during TNF-alpha-induced signaling","volume":"22","author":"Gupta","year":"2002","journal-title":"Journal of Clinical Immunology"},{"issue":"3","key":"10.1002\/humu.23693-BIB0015|humu23693-cit-0015","first-page":"879\u2212886","article-title":"MG132, a proteasome inhibitor, induced death of calf pulmonary artery endothelial cells via caspase-dependent apoptosis and GSH depletion","volume":"30","author":"Han","year":"2010","journal-title":"Anticancer Research"},{"issue":"3","key":"10.1002\/humu.23693-BIB0016|humu23693-cit-0016","doi-asserted-by":"crossref","first-page":"369\u2212381","DOI":"10.1016\/j.mito.2011.01.010","article-title":"The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: From respiration to apoptosis","volume":"11","author":"Huttemann","year":"2011","journal-title":"Mitochondrion"},{"issue":"2","key":"10.1002\/humu.23693-BIB0017|humu23693-cit-0017","doi-asserted-by":"crossref","first-page":"278\u2212286","DOI":"10.1016\/S0006-291X(03)00734-4","article-title":"Early embryonic lethality caused by targeted disruption of the mouse PHGPx gene","volume":"305","author":"Imai","year":"2003","journal-title":"Biochemical and Biophysical Research Communications"},{"issue":"1","key":"10.1002\/humu.23693-BIB0018|humu23693-cit-0018","doi-asserted-by":"crossref","first-page":"E13","DOI":"10.3390\/antiox7010013","article-title":"Reactive oxygen species and mitochondrial dynamics: The Yin and Yang of mitochondrial dysfunction and cancer progression","volume":"7","author":"Jezek","year":"2018","journal-title":"Antioxidants"},{"issue":"6","key":"10.1002\/humu.23693-BIB0019|humu23693-cit-0019","doi-asserted-by":"crossref","first-page":"600\u2212607","DOI":"10.1038\/gim.2015.139","article-title":"Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing","volume":"18","author":"Kancheva","year":"2016","journal-title":"Genetics in Medicine"},{"key":"10.1002\/humu.23693-BIB0020|humu23693-cit-0020","first-page":"193\u2212214","article-title":"The function of cytidine coenzymes in the biosynthesis of phospholipids","volume":"222","author":"Kennedy","year":"1965","journal-title":"Journal of Biological Chemistry"},{"issue":"Pt 1","key":"10.1002\/humu.23693-BIB0021|humu23693-cit-0021","first-page":"33\u221238","article-title":"Post-translational processing of the phosphatidylserine decarboxylase gene product in Chinese hamster ovary cells","volume":"319","author":"Kuge","year":"1996","journal-title":"Biochemical Journal"},{"issue":"14","key":"10.1002\/humu.23693-BIB0022|humu23693-cit-0022","doi-asserted-by":"crossref","first-page":"1754\u22121760","DOI":"10.1093\/bioinformatics\/btp324","article-title":"Fast and accurate short read alignment with Burrows-Wheeler transform","volume":"25","author":"Li","year":"2009","journal-title":"Bioinformatics"},{"issue":"9","key":"10.1002\/humu.23693-BIB0023|humu23693-cit-0023","doi-asserted-by":"crossref","first-page":"1297\u22121303","DOI":"10.1101\/gr.107524.110","article-title":"The genome analysis toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data","volume":"20","author":"McKenna","year":"2010","journal-title":"Genome Research"},{"issue":"5","key":"10.1002\/humu.23693-BIB0024|humu23693-cit-0024","doi-asserted-by":"crossref","first-page":"e1004311","DOI":"10.1371\/journal.pgen.1004311","article-title":"The impairment of MAGMAS function in human is responsible for a severe skeletal dysplasia","volume":"10","author":"Mehawej","year":"2014","journal-title":"PLoS Genetics"},{"issue":"1","key":"10.1002\/humu.23693-BIB0025|humu23693-cit-0025","doi-asserted-by":"crossref","first-page":"30\u221237","DOI":"10.1111\/cge.12792","article-title":"Spondyloepimetaphyseal dysplasia with neurodegeneration associated with AIFM1 mutation-a novel phenotype of the mitochondrial disease","volume":"91","author":"Mierzewska","year":"2017","journal-title":"Clinical Genetics"},{"issue":"1","key":"10.1002\/humu.23693-BIB0026|humu23693-cit-0026","doi-asserted-by":"crossref","first-page":"30\u221235","DOI":"10.1038\/ng.499","article-title":"Exome sequencing identifies the cause of a mendelian disorder","volume":"42","author":"Ng","year":"2010","journal-title":"Nature Genetics"},{"issue":"12","key":"10.1002\/humu.23693-BIB0027|humu23693-cit-0027","doi-asserted-by":"crossref","first-page":"1256\u22121261","DOI":"10.1038\/ng.1004","article-title":"Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome","volume":"43","author":"Pansuriya","year":"2011","journal-title":"Nature Genetics"},{"issue":"2","key":"10.1002\/humu.23693-BIB0028|humu23693-cit-0028","doi-asserted-by":"crossref","first-page":"484\u2212494","DOI":"10.1016\/0003-9861(83)90613-6","article-title":"Characterization of brain phosphatidylserine decarboxylase: Localization in the mitochondrial inner membrane","volume":"223","author":"Percy","year":"1983","journal-title":"Archives of Biochemistry and Biophysics"},{"issue":"8","key":"10.1002\/humu.23693-BIB0029|humu23693-cit-0029","first-page":"1300\u22121306","article-title":"Emerging role of Lon protease as a master regulator of mitochondrial functions","volume":"1857","author":"Pinti","year":"2016","journal-title":"Biochimica et Biophysica Acta"},{"issue":"1","key":"10.1002\/humu.23693-BIB0030|humu23693-cit-0030","first-page":"259\u2212265","article-title":"Proteasome inhibitors induce cytochrome c-caspase-3-like protease-mediated apoptosis in cultured cortical neurons","volume":"20","author":"Qui","year":"2000","journal-title":"The Journal of Neuroscience"},{"issue":"3","key":"10.1002\/humu.23693-BIB0031|humu23693-cit-0031","doi-asserted-by":"crossref","first-page":"459\u2212468","DOI":"10.1089\/ars.2010.3363","article-title":"Mitochondrial ROS generation and its regulation: Mechanisms involved in H(2)O(2) signaling","volume":"14","author":"Rigoulet","year":"2011","journal-title":"Antioxidants & Redox Signaling"},{"issue":"3","key":"10.1002\/humu.23693-BIB0032|humu23693-cit-0032","doi-asserted-by":"crossref","first-page":"499\u2212508","DOI":"10.1038\/cdd.2014.219","article-title":"Phosphatidylethanolamine positively regulates autophagy and longevity","volume":"22","author":"Rockenfeller","year":"2015","journal-title":"Cell Death & Differentiation"},{"key":"10.1002\/humu.23693-BIB0033|humu23693-cit-0033","doi-asserted-by":"crossref","first-page":"17154","DOI":"10.1038\/srep17154","article-title":"Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia","volume":"5","author":"Royer-Bertrand","year":"2015","journal-title":"Scientific Reports"},{"issue":"2","key":"10.1002\/humu.23693-BIB0034|humu23693-cit-0034","doi-asserted-by":"crossref","first-page":"151\u2212162","DOI":"10.1002\/iub.159","article-title":"Phosphatidylserine decarboxylases, key enzymes of lipid metabolism","volume":"61","author":"Schuiki","year":"2009","journal-title":"IUBMB Life"},{"issue":"3","key":"10.1002\/humu.23693-BIB0035|humu23693-cit-0035","doi-asserted-by":"crossref","first-page":"237\u2212248","DOI":"10.1016\/j.cmet.2008.07.005","article-title":"Glutathione peroxidase 4 senses and translates oxidative stress into 12\/15-lipoxygenase dependent- and AIF-mediated cell death","volume":"8","author":"Seiler","year":"2008","journal-title":"Cell Metabolism"},{"issue":"7","key":"10.1002\/humu.23693-BIB0036|humu23693-cit-0036","doi-asserted-by":"crossref","first-page":"470\u2212474","DOI":"10.1136\/jmedgenet-2013-102218","article-title":"Mutations in the enzyme glutathione peroxidase 4 cause Sedaghatian-type spondylometaphyseal dysplasia","volume":"51","author":"Smith","year":"2014","journal-title":"Journal of Medical Genetics"},{"issue":"48","key":"10.1002\/humu.23693-BIB0037|humu23693-cit-0037","doi-asserted-by":"crossref","first-page":"40032\u221240040","DOI":"10.1074\/jbc.M506510200","article-title":"Disruption of the phosphatidylserine decarboxylase gene in mice causes embryonic lethality and mitochondrial defects","volume":"280","author":"Steenbergen","year":"2005","journal-title":"Journal of Biological Chemistry"},{"issue":"1","key":"10.1002\/humu.23693-BIB0038|humu23693-cit-0038","doi-asserted-by":"crossref","first-page":"121\u2212135","DOI":"10.1016\/j.ajhg.2014.12.003","article-title":"CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease","volume":"96","author":"Strauss","year":"2015","journal-title":"The American Journal of Human Genetics"},{"issue":"6","key":"10.1002\/humu.23693-BIB0039|humu23693-cit-0039","first-page":"2459\u22122466","article-title":"Induction of the mitochondrial permeability transition mediates the killing of HeLa cells by staurosporine","volume":"61","author":"Tafani","year":"2001","journal-title":"Cancer Research"},{"issue":"6","key":"10.1002\/humu.23693-BIB0040|humu23693-cit-0040","doi-asserted-by":"crossref","first-page":"4158\u22124173","DOI":"10.1074\/jbc.M112.434183","article-title":"Phosphatidylethanolamine deficiency in Mammalian mitochondria impairs oxidative phosphorylation and alters mitochondrial morphology","volume":"288","author":"Tasseva","year":"2013","journal-title":"Journal of Biological Chemistry"},{"issue":"9","key":"10.1002\/humu.23693-BIB0041|humu23693-cit-0041","doi-asserted-by":"crossref","first-page":"2404\u22122417","DOI":"10.1016\/j.celrep.2018.07.101","article-title":"Mitochondrial complex I activity is required for maximal autophagy","volume":"24","author":"Thomas","year":"2018","journal-title":"Cell Reports"},{"issue":"3","key":"10.1002\/humu.23693-BIB0042|humu23693-cit-0042","first-page":"543\u2212554","article-title":"Formation and function of phosphatidylserine and phosphatidylethanolamine in mammalian cells","volume":"1831","author":"Vance","year":"2013","journal-title":"Biochimica et Biophysica Acta"},{"issue":"20","key":"10.1002\/humu.23693-BIB0043|humu23693-cit-0043","doi-asserted-by":"crossref","first-page":"5317\u22125326","DOI":"10.1111\/j.1742-4658.2005.04928.x","article-title":"Human mitochondrial complex I assembly is mediated by NDUFAF1","volume":"272","author":"Vogel","year":"2005","journal-title":"The FEBS Journal"},{"issue":"2","key":"10.1002\/humu.23693-BIB0044|humu23693-cit-0044","doi-asserted-by":"crossref","first-page":"105\u2212117","DOI":"10.1016\/j.tem.2015.12.001","article-title":"Mitochondrial dynamics and metabolic regulation","volume":"27","author":"Wai","year":"2016","journal-title":"Trends in Endocrinology & Metabolism"},{"issue":"16","key":"10.1002\/humu.23693-BIB0045|humu23693-cit-0045","doi-asserted-by":"crossref","first-page":"e164","DOI":"10.1093\/nar\/gkq603","article-title":"ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data","volume":"38","author":"Wang","year":"2010","journal-title":"Nucleic Acids Research"},{"issue":"38","key":"10.1002\/humu.23693-BIB0046|humu23693-cit-0046","first-page":"E3976\u2212E3985","article-title":"Phosphatidylethanolamine deficiency disrupts \u03b1-synuclein homeostasis in yeast and worm models of Parkinson disease","volume":"1111","author":"Wang","year":"2014","journal-title":"Proceedings of the National Academy of Sciences of the United States of America"},{"issue":"1-3","key":"10.1002\/humu.23693-BIB0047|humu23693-cit-0047","doi-asserted-by":"crossref","first-page":"101\u2212105","DOI":"10.1016\/S0014-5793(02)03151-4","article-title":"Proteasome inhibitors stimulate activator protein-1 pathway via reactive oxygen species production","volume":"526","author":"Wu","year":"2002","journal-title":"FEBS Letters"},{"issue":"10","key":"10.1002\/humu.23693-BIB0048|humu23693-cit-0048","doi-asserted-by":"crossref","first-page":"1556\u22121566","DOI":"10.1038\/nprot.2015.105","article-title":"Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR","volume":"10","author":"Yang","year":"2015","journal-title":"Nature Protocols"},{"issue":"4","key":"10.1002\/humu.23693-BIB0049|humu23693-cit-0049","doi-asserted-by":"crossref","first-page":"496\u2212502","DOI":"10.1016\/S0891-5849(02)01360-6","article-title":"The selenoprotein GPX4 is essential for mouse development and protects from radiation and oxidative damage insults","volume":"34","author":"Yant","year":"2003","journal-title":"Free Radical Biology and Medicine"}],"container-title":["Human Mutation"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fhumu.23693","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1002\/humu.23693\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,12,29]],"date-time":"2022-12-29T16:57:20Z","timestamp":1672333040000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/humu.23693"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,12,21]]},"references-count":49,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2019,3]]}},"URL":"https:\/\/doi.org\/10.1002\/humu.23693","archive":["Portico"],"relation":{},"ISSN":["1059-7794"],"issn-type":[{"value":"1059-7794","type":"print"}],"subject":[],"published":{"date-parts":[[2018,12,21]]}}}