{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T02:28:28Z","timestamp":1780367308295,"version":"3.54.1"},"reference-count":34,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2015,12,1]],"date-time":"2015-12-01T00:00:00Z","timestamp":1448928000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Neurogenetics"],"published-print":{"date-parts":[[2016,1]]},"DOI":"10.1007\/s10048-015-0468-7","type":"journal-article","created":{"date-parts":[[2015,12,1]],"date-time":"2015-12-01T05:45:52Z","timestamp":1448948752000},"page":"71-78","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":21,"title":["Refining the phenotype associated with CASC5 mutation"],"prefix":"10.1007","volume":"17","author":[{"given":"Abdelkrim","family":"Saadi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Florine","family":"Verny","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Karine","family":"Siquier-Pernet","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christine","family":"Bole-Feysot","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patrick","family":"Nitschke","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Arnold","family":"Munnich","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Myriam","family":"Abada-Dendib","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Malika","family":"Chaouch","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marc","family":"Abramowicz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laurence","family":"Colleaux","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2015,12,1]]},"reference":[{"issue":"5","key":"468_CR1","doi-asserted-by":"crossref","first-page":"717","DOI":"10.1086\/429930","volume":"76","author":"CG Woods","year":"2005","unstructured":"Woods CG, Bond J, Enard W (2005) Autosomal recessive primary microcephaly MCPH a review of clinical, molecular, and evolutionary findings. Am J Hum Genet 76(5):717\u2013728","journal-title":"Am J Hum Genet"},{"issue":"3","key":"468_CR2","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1016\/j.pneurobio.2009.11.002","volume":"90","author":"AM Kaindl","year":"2010","unstructured":"Kaindl AM, Passemard S, Kumar P, Kraemer N, Issa L, Zwirner A, Gerard B, Verloes A, Mani S, Gressens P (2010) Many roads lead to primary autosomal recessive microcephaly. Prog Neurobiol 90(3):363\u2013383. doi: 10.1016\/j.pneurobio.2009.11.002","journal-title":"Prog Neurobiol"},{"issue":"12","key":"468_CR3","doi-asserted-by":"crossref","first-page":"823","DOI":"10.1136\/jmg.2009.076398","volume":"47","author":"H Darvish","year":"2010","unstructured":"Darvish H, Esmaeeli-Nieh MGB, Mohseni M, Ghasemi-Firouzabadi S et al (2010) A clinical and molecular genetics study of 112 Iranian families with primary microcephaly. J Med Genet 47(12):823\u2013828. doi: 10.1136\/jmg.2009.076398","journal-title":"J Med Genet"},{"issue":"9","key":"468_CR4","doi-asserted-by":"crossref","first-page":"2071","DOI":"10.1002\/ajmg.a.34165","volume":"155A","author":"DR Murdock","year":"2011","unstructured":"Murdock DR, Clark GD, Bainbridge MN, Newsham I, Wu YQ, Muzny DM, Cheung SW, Gibbs RA, Ramocki MB (2011) Whole\u2013exome sequencing identifies compound heterozygous mutations in WDR62 insiblings with recurrent polymicrogyria. Am J Med Genet A 155A(9):2071\u20132077. doi: 10.1002\/ajmg.a.34165","journal-title":"Am J Med Genet A"},{"issue":"11","key":"468_CR5","doi-asserted-by":"crossref","first-page":"1015","DOI":"10.1038\/ng.683","volume":"42","author":"TW Yu","year":"2010","unstructured":"Yu TW, Mochida GH, Tischfield DJ, Sgaier SK, Flores-Sarnat L, Sergi CM, Top\u00e7u M, McDonald MT, Barry BJ, Felie JM, Sunu C, Dobyns WB, Folkerth RD, Barkovich AJ, Walsh CA (2010) Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nat Genet 42(11):1015\u20131020. doi: 10.1038\/ng.683","journal-title":"Nat Genet"},{"issue":"10","key":"468_CR6","doi-asserted-by":"crossref","first-page":"718","DOI":"10.1136\/jmg.39.10.718","volume":"39","author":"E Roberts","year":"2002","unstructured":"Roberts E, Hampshire DJ, Pattison L, Springell K, Jafri H, Corry P, Mannon J, Rashid Y, Crow Y, Bond J, Woods CG (2002) Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation. J Med Genet 39(10):718\u2013721","journal-title":"J Med Genet"},{"issue":"9","key":"468_CR7","doi-asserted-by":"crossref","first-page":"725","DOI":"10.1136\/jmg.2004.027706","volume":"42","author":"J Shen","year":"2005","unstructured":"Shen J, Eyaid W, Mochida GH, Al-Moayyad F, Bodell A, Woods CG, Walsh CA (2005) ASPM mutations identified in patients with primary microcephaly and seizures. J Med Genet 42(9):725\u2013729","journal-title":"J Med Genet"},{"issue":"12","key":"468_CR8","doi-asserted-by":"crossref","first-page":"962","DOI":"10.1212\/WNL.0b013e3181b8799a","volume":"73","author":"S Passemard","year":"2009","unstructured":"Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, De Villemeur TB, Boespflug-Tanguy O, Burglen L et al (2009) Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. Neurology 73(12):962\u2013969. doi: 10.1212\/WNL.0b013e3181b8799a","journal-title":"Neurology"},{"issue":"4","key":"468_CR9","doi-asserted-by":"crossref","first-page":"1015","DOI":"10.1086\/339518","volume":"70","author":"H Neitzel","year":"2002","unstructured":"Neitzel H, Neumann LM, Schindler D, Wirges A, Tonnies H, Trimborn M, Krebsova A, Richter R, Sperling K (2002) Premature chromosome condensation inhumans associated with microcephaly and mental retardation: a novel autosomal recessive condition. Am J Hum Genet 70(4):1015\u20131022","journal-title":"Am J Hum Genet"},{"issue":"2","key":"468_CR10","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1086\/422855","volume":"75","author":"M Trimborn","year":"2004","unstructured":"Trimborn M, Bell SM, Felix C, Rashid Y, Jafri H, Griffiths PD, Neumann LM, Krebs A, Reis A, Sperling K, Neitzel H, Jackson AP (2004) Mutations in microcephalin cause aberrant regulation of chromosome condensation. Am J Hum Genet 75(2):261\u2013266","journal-title":"Am J Hum Genet"},{"issue":"11","key":"468_CR11","doi-asserted-by":"crossref","first-page":"1439","DOI":"10.1002\/ajmg.a.32312","volume":"146A","author":"J Desir","year":"2008","unstructured":"Desir J, Cassart M, David P, Van Bogaert P, Abramowicz M (2008) Primary microcephaly with ASPM mutation shows simplified cortical gyration with anteroposterior gradient pre- and post-natally. Am J Med Genet A 146A(11):1439\u20131443. doi: 10.1002\/ajmg.a.32312","journal-title":"Am J Med Genet A"},{"issue":"4","key":"468_CR12","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1016\/j.ejmg.2009.03.013","volume":"52","author":"A Saadi","year":"2009","unstructured":"Saadi A, Borck G, Boddaert N, Chekkour MC, Imessaoudene B, Munnich A, Colleaux L, Chaouch M (2009) Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. Eur J Med Genet 52(4):180\u2013184. doi: 10.1016\/j.ejmg.2009.03.013","journal-title":"Eur J Med Genet"},{"issue":"7312","key":"468_CR13","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1038\/nature09327","volume":"467","author":"K Bilg\u00fcvar","year":"2010","unstructured":"Bilg\u00fcvar K, Ozt\u00fcrk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizo\u011flu D, T\u00fcys\u00fcz B, Ca\u011flayan AO, G\u00f6kben S, Kaymak\u00e7alan H, Barak T, Bakircio\u011flu M, Yasuno K, Ho W, Sanders S, Zhu Y et al (2010) Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature 467(7312):207\u2013210. doi: 10.1038\/nature09327","journal-title":"Nature"},{"issue":"6","key":"468_CR14","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1111\/j.1399-0004.2011.01686.x","volume":"80","author":"V Bhat","year":"2011","unstructured":"Bhat V, Girimaji SC, Mohan G, Arvinda HR, Singhmar P, Duvvari MR, Kumar A (2011) Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations. Clin Genet 80(6):532\u2013540. doi: 10.1111\/j.1399-0004.2011.01686.x","journal-title":"Clin Genet"},{"issue":"1","key":"468_CR15","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1086\/341283","volume":"71","author":"AP Jackson","year":"2002","unstructured":"Jackson AP, Eastwood H, Bell SM, Adu J, Toomes C, Carr IM, Roberts E, Hampshire DJ, Crow YJ, Mighell AJ, Karbani G, Jafri H, Rashid Y, Mueller RF, Markham AF, Woods CG (2002) Identification of microcephalin, a protein implicated in determining the size of the human brain. Am J Hum Genet 71(1):136\u2013142","journal-title":"Am J Hum Genet"},{"issue":"11","key":"468_CR16","doi-asserted-by":"crossref","first-page":"1010","DOI":"10.1038\/ng.682","volume":"42","author":"AK Nicholas","year":"2010","unstructured":"Nicholas AK, Khurshid M, D\u00e9sir J, Carvalho OP, Cox JJ, Thornton G, Kausar R, Ansar M, Ahmad W, Verloes A, Passemard S, Misson JP, Lindsay S, Gergely F, Dobyns WB, Roberts E, Abramowicz M, Woods CG (2010) WDR62 is associated with the spindle pole and is mutated in human microcephaly. Nat Genet 42(11):1010\u20131014. doi: 10.1038\/ng.682","journal-title":"Nat Genet"},{"issue":"4","key":"468_CR17","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1038\/ng1539","volume":"37","author":"J Bond","year":"2005","unstructured":"Bond J, Roberts E, Springell K, Lizarraga SB, Scott S, Higgins J, Hampshire DJ, Morrison EE, Leal GF, Silva EO, Costa SM, Baralle D, Raponi M, Karbani G, Rashid Y, Jafri H, Bennett C, Corry P, Walsh CA, Woods CG (2005) A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Nat Genet 37(4):353\u2013355","journal-title":"Nat Genet"},{"issue":"24","key":"468_CR18","doi-asserted-by":"crossref","first-page":"5306","DOI":"10.1093\/hmg\/dds386","volume":"21","author":"A Genin","year":"2012","unstructured":"Genin A, Desir J, Lambert N, Biervliet M, Van Der Aa N, Pierquin G, Killian A, Tosi M, Urbina M, Lefort A, Libert F, Pirson I, Abramowicz M (2012) Kinetochore KMN network gene CASC5 mutated in primary microcephaly. Hum Mol Genet 21(24):5306\u20135317. doi: 10.1093\/hmg\/dds386","journal-title":"Hum Mol Genet"},{"issue":"2","key":"468_CR19","doi-asserted-by":"crossref","first-page":"316","DOI":"10.1038\/ng995","volume":"32","author":"J Bond","year":"2002","unstructured":"Bond J, Roberts E, Mochida GH, Hampshire DJ, Scott S, Askham JM, Springell K, Mahadevan M, Crow YJ, Markham AF, Walsh CA, Woods CG (2002) ASPM is a major determinant of cerebral cortical size. Nat Genet 32(2):316\u2013320","journal-title":"Nat Genet"},{"issue":"2","key":"468_CR20","doi-asserted-by":"crossref","first-page":"286","DOI":"10.1016\/j.ajhg.2009.01.017","volume":"84","author":"A Kumar","year":"2009","unstructured":"Kumar A, Girimaji SC, Duvvari MR, Blanton SH (2009) Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly. Am J Hum Genet 84(2):286\u2013290. doi: 10.1016\/j.ajhg.2009.01.017","journal-title":"Am J Hum Genet"},{"issue":"5","key":"468_CR21","doi-asserted-by":"crossref","first-page":"871","DOI":"10.1016\/j.ajhg.2012.03.016","volume":"90","author":"MS Hussain","year":"2012","unstructured":"Hussain MS, Baig SM, Neumann S, N\u00fcrnberg G, Farooq M, Ahmad I, Alef T, Hennies HC, Technau M, Altm\u00fcller J, Frommolt P, Thiele H, Noegel AA, N\u00fcrnberg P (2012) A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function. Am J Hum Genet 90(5):871\u2013878. doi: 10.1016\/j.ajhg.2012.03.016","journal-title":"Am J Hum Genet"},{"issue":"1","key":"468_CR22","doi-asserted-by":"crossref","first-page":"40","DOI":"10.1016\/j.ajhg.2010.06.003","volume":"87","author":"DL Guernsey","year":"2010","unstructured":"Guernsey DL, Jiang H, Hussin J, Arnold M, Bouyakdan K, Perry S, Babineau-Sturk T, Beis J, Dumas N, Evans SC, Ferguson M, Matsuoka M, Macgillivray C, Nightingale M, Patry L, Rideout AL, Thomas A, Orr A, Hoffmann I, Michaud JL, Awadalla P, Meek DC, Ludman M, Samuels ME (2010) Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4. Am J Hum Genet 87(1):40\u201351. doi: 10.1016\/j.ajhg.2010.06.003","journal-title":"Am J Hum Genet"},{"issue":"5","key":"468_CR23","doi-asserted-by":"crossref","first-page":"1097","DOI":"10.1016\/j.cell.2012.10.043","volume":"151","author":"YJ Yang","year":"2012","unstructured":"Yang YJ, Baltus AE, Mathew RS, Murphy EA, Evrony GD, Gonzalez DM, Wang EP, Marshall-Walker CA, Barry BJ, Murn J, Tatarakis A, Mahajan MA, Samuels HH, Shi Y, Golden JA, Mahajnah M, Shenhav R, Walsh CA (2012) Microcephaly gene links trithorax and REST\/NRSF to control neural stem cell proliferation and differentiation. Cell 151(5):1097\u20131112. doi: 10.1016\/j.cell.2012.10.043","journal-title":"Cell"},{"issue":"11","key":"468_CR24","doi-asserted-by":"crossref","first-page":"2200","DOI":"10.1093\/hmg\/ddt072","volume":"22","author":"S Awad","year":"2013","unstructured":"Awad S, Al-Dosari MS, Alyacoub N, Colak D, Salih MA, Alkuraya FS, Poizat C (2013) Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis. Hum Mol Genet 22(11):2200\u20132213. doi: 10.1093\/hmg\/ddt072","journal-title":"Hum Mol Genet"},{"issue":"25","key":"468_CR25","doi-asserted-by":"crossref","first-page":"5199","DOI":"10.1093\/hmg\/ddt374","volume":"22","author":"MS Hussain","year":"2013","unstructured":"Hussain MS, Baig SM, Neumann S, Peche VS, Szczepanski S, N\u00fcrnberg G, Tariq M, Jameel M, Naeem T, Fatima A, Malik NA, Ahmad I, Altm\u00fcller J, Frommolt P, Thiele H, H\u00f6hne W, Yigit G, Wollnik B, Neubauer BA, N\u00fcrnberg P, Noegel AA (2013) CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly. Hum Mol Genet 22(25):5199\u20135214. doi: 10.1093\/hmg\/ddt374","journal-title":"Hum Mol Genet"},{"issue":"2","key":"468_CR26","doi-asserted-by":"crossref","first-page":"587","DOI":"10.1091\/mbc.E07-10-1051","volume":"19","author":"IM Cheeseman","year":"2008","unstructured":"Cheeseman IM, Hori T, Fukagawa T, Desai A (2008) KNL1 and the CENP-H\/I\/K complex coordinately direct kinetochore assembly in vertebrates. Mol Biol Cell 19(2):587\u2013594","journal-title":"Mol Biol Cell"},{"issue":"11\u201312","key":"468_CR27","doi-asserted-by":"crossref","first-page":"1691","DOI":"10.1016\/j.str.2011.09.017","volume":"19","author":"VM Bolanos-Garcia","year":"2011","unstructured":"Bolanos-Garcia VM, Lischetti T, Matak-Vinkovic D et al (2011) Structure of a Blinkin-BUBR1 complex reveals an interaction crucial for kinetochore-mitotic checkpoint regulation via an unanticipated binding Site,\u201d. Structure 19(11\u201312):1691\u20131700. doi: 10.1016\/j.str.2011.09.017","journal-title":"Structure"},{"issue":"4","key":"468_CR28","doi-asserted-by":"crossref","first-page":"266","DOI":"10.1136\/jmg.39.4.266","volume":"39","author":"M Rio","year":"2002","unstructured":"Rio M, Molinari F, Heuertz S, Ozilou C, Gosset P, Raoul O, Cormier-Daire V, Amiel J, Lyonnet S, Le Merrer M, Turleau C, de Blois MC, Prieur M, Romana S, Vekemans M, Munnich A, Colleaux L (2002) Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. J Med Genet 39(4):266\u2013270","journal-title":"J Med Genet"},{"issue":"5","key":"468_CR29","doi-asserted-by":"crossref","first-page":"998","DOI":"10.1128\/MCB.00815-10","volume":"31","author":"T Kiyomitsu","year":"2011","unstructured":"Kiyomitsu T, Murakami H, Yanagida M (2011) Protein interaction domain mapping of human kinetochore protein Blinkin reveals a consensus motif for binding of spindle assembly checkpoint proteins Bub1 and BubR1. Mol Cell Biol 31(5):998\u20131011. doi: 10.1128\/MCB.00815-10","journal-title":"Mol Cell Biol"},{"issue":"5","key":"468_CR30","doi-asserted-by":"crossref","first-page":"835","DOI":"10.1083\/jcb.201002070","volume":"190","author":"A Petrovic","year":"2010","unstructured":"Petrovic A, Pasqualato S, Dube P, Krenn V, Santaguida S, Cittaro D, Monzani S, Massimiliano L, Keller J, Tarricone A, Maiolica A, Stark H, Musacchio A (2010) The MIS12 complex is a protein interaction hub for outer kinetochore assembly. J Cell Biol 190(5):835\u2013852. doi: 10.1083\/jcb.201002070","journal-title":"J Cell Biol"},{"issue":"6","key":"468_CR31","doi-asserted-by":"crossref","first-page":"411","DOI":"10.1136\/jmg.2009.076646","volume":"47","author":"MS Al-Dosari","year":"2010","unstructured":"Al-Dosari MS, Shaheen R, Colak D, Alkuraya FS (2010) Novel CENPJ mutation causes Seckel syndrome. J Med Genet 47(6):411\u2013414. doi: 10.1136\/jmg.2009.076646","journal-title":"J Med Genet"},{"issue":"1","key":"468_CR32","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1038\/ng.725","volume":"43","author":"E Kalay","year":"2011","unstructured":"Kalay E, Yigit G, Aslan Y, Brown KE, Pohl E, Bicknell LS, Kayserili H, Li Y, T\u00fcys\u00fcz B, N\u00fcrnberg G, Kiess W, Koegl M, Baessmann I, Buruk K, Toraman B, Kayipmaz S, Kul S, Ikbal M, Turner DJ, Taylor MS, Aerts J, Scott C, Milstein K, Dollfus H, Wieczorek D, Brunner HG, Hurles M, Jackson AP, Rauch A, N\u00fcrnberg P, Karag\u00fczel A, Wollnik B (2011) CEP152 is a genome maintenance protein disrupted in Seckel syndrome. Nat Genet 43(1):23\u201326. doi: 10.1038\/ng.725","journal-title":"Nat Genet"},{"issue":"8","key":"468_CR33","doi-asserted-by":"crossref","first-page":"1023","DOI":"10.1007\/s00439-014-1443-3","volume":"133","author":"GM Mirzaa","year":"2014","unstructured":"Mirzaa GM, Vitre B, Carpenter G, Abramowicz I, Gleeson JG, Pachiorkowski AR, Cleveland DW, Dobyns WB, O'Driscoll M (2014) Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism. Hum Genet 133(8):1023\u20131039. doi: 10.1007\/s00439-014-1443-3","journal-title":"Hum Genet"},{"issue":"9","key":"468_CR34","doi-asserted-by":"crossref","first-page":"2161","DOI":"10.1002\/ajmg.a.36611","volume":"164A","author":"CJ Poulton","year":"2014","unstructured":"Poulton CJ, Schot R, Seufert K, Lequin MH, Accogli A, Annunzio GD, Villard L, Philip N, de Coo R, Catsman-Berrevoets C, Grasshoff U, Kattentidt-Mouravieva A, Calf H, de Vreugt-Gronloh E, van Unen L, Verheijen FW, Galjart N, Morris-Rosendahl DJ, Mancini GM (2014) Severe presentation of WDR62 mutation: is there a role for modifying genetic factors? Am J Med Genet A 164A(9):2161\u20132171. doi: 10.1002\/ajmg.a.36611","journal-title":"Am J Med Genet A"}],"container-title":["neurogenetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10048-015-0468-7.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10048-015-0468-7\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10048-015-0468-7","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,29]],"date-time":"2019-05-29T08:01:07Z","timestamp":1559116867000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10048-015-0468-7"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,12,1]]},"references-count":34,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2016,1]]}},"alternative-id":["468"],"URL":"https:\/\/doi.org\/10.1007\/s10048-015-0468-7","relation":{},"ISSN":["1364-6745","1364-6753"],"issn-type":[{"value":"1364-6745","type":"print"},{"value":"1364-6753","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015,12,1]]}}}