Clinical and Genetic Features of Biallelic Mutations in SORD in a Series of Chinese Patients With Charcot-Marie-Tooth and Distal Hereditary Motor Neuropathy

Biallelic mutations in the sorbitol dehydrogenase (SORD) gene have recently been found to be one of the most frequent causes of autosomal recessive axonal Charcot-Marie-Tooth (CMT2) and distal hereditary motor neuropathy (dHMN). This study was performed to explore the frequency of SORD mutations and...

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Detalles Bibliográficos
Autores principales: Liu, Xiaoxuan, He, Ji, Yilihamu, Mubalake, Duan, Xiaohui, Fan, Dongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607551/
https://www.ncbi.nlm.nih.gov/pubmed/34819907
http://dx.doi.org/10.3389/fneur.2021.733926

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607551/
https://www.ncbi.nlm.nih.gov/pubmed/34819907
http://dx.doi.org/10.3389/fneur.2021.733926

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