Journal article

Mutation in CEP135 causing primary microcephaly and subcortical heterotopia


Authors listBamborschke, Daniel; Daimagueler, Huelya-Sevcan; Hahn, Andreas; Hussain, Muhammad S.; Nuernberg, Peter; Cirak, Sebahattin

Publication year2020

Pages2450-2453

JournalThe American Journal of Medical Genetics - Part A

Volume number182

Issue number10

ISSN1552-4825

eISSN1552-4833

Open access statusHybrid

DOI Linkhttps://doi.org/10.1002/ajmg.a.61762

PublisherWiley



Citation Styles

Harvard Citation styleBamborschke, D., Daimagueler, H., Hahn, A., Hussain, M., Nuernberg, P. and Cirak, S. (2020) Mutation in CEP135 causing primary microcephaly and subcortical heterotopia, The American Journal of Medical Genetics - Part A, 182(10), pp. 2450-2453. https://doi.org/10.1002/ajmg.a.61762

APA Citation styleBamborschke, D., Daimagueler, H., Hahn, A., Hussain, M., Nuernberg, P., & Cirak, S. (2020). Mutation in CEP135 causing primary microcephaly and subcortical heterotopia. The American Journal of Medical Genetics - Part A. 182(10), 2450-2453. https://doi.org/10.1002/ajmg.a.61762



Keywords


CEP135CPAPMALFORMATIONSneuronal migration defectprimary microcephalySUBCORTICAL HETEROTOPIAVARIANTSWDR62

Last updated on 2025-10-06 at 11:13