Case report: Genotype and phenotype of DYNC1H1-related malformations of cortical development: a case report and literature review

Case report: Genotype and phenotype of DYNC1H1-related malformations of cortical development: a case report and literature review

BackgroundMutations in the dynein cytoplasmic 1 heavy chain 1 (DYNC1H1) gene are linked to malformations of cortical development (MCD), which may be accompanied by central nervous system (CNS) manifestations. Here, we present the case of a patient with MCD harboring a variant of DYNC1H1 and review t...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Wen-Rong Ge, Pei-Pei Fu, Wei-Na Zhang, Bo Zhang, Ying-Xue Ding, Guang Yang
التنسيق:	مقال
اللغة:	English
منشور في:	Frontiers Media S.A. 2023-04-01
سلاسل:	Frontiers in Neurology
الموضوعات:	DYNC1H1 gene malformations of cortical development variant microtubule-binding domain case report
الوصول للمادة أونلاين:	https://www.frontiersin.org/articles/10.3389/fneur.2023.1163803/full

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