Journalartikel

Mutation in CEP135 causing primary microcephaly and subcortical heterotopia


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

Jahr der Veröffentlichung2020

Seiten2450-2453

ZeitschriftThe American Journal of Medical Genetics - Part A

Bandnummer182

Heftnummer10

ISSN1552-4825

eISSN1552-4833

Open Access StatusHybrid

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

VerlagWiley



Zitierstile

Harvard-ZitierstilBamborschke, 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-ZitierstilBamborschke, 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



Schlagwörter


CEP135CPAPMALFORMATIONSneuronal migration defectprimary microcephalySUBCORTICAL HETEROTOPIAVARIANTSWDR62


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