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...
Hauptverfasser: | Wen-Rong Ge, Pei-Pei Fu, Wei-Na Zhang, Bo Zhang, Ying-Xue Ding, Guang Yang |
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Format: | Artikel |
Sprache: | English |
Veröffentlicht: |
Frontiers Media S.A.
2023-04-01
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Schriftenreihe: | Frontiers in Neurology |
Schlagworte: | |
Online Zugang: | https://www.frontiersin.org/articles/10.3389/fneur.2023.1163803/full |
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