Two Novel Myelin Protein Zero Mutations in a Group of Chinese Patients

Mutations in the myelin protein zero gene are responsible for the autosomal dominant Charcot-Marie-Tooth disease (CMT). We summarized the genetic and clinical features of six unrelated Chinese families and the genetic spectrum of Chinese patients with myelin protein zero (MPZ) mutations. Our study r...

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Detalles Bibliográficos
Autores principales: Chen, Bin, Zhang, Zaiqiang, Chen, Na, Li, Wei, Pan, Hua, Wang, Xingao, Ren, Yuting, Shi, Yuzhi, Tai, Hongfei, Niu, Songtao
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/PMC8674198/
https://www.ncbi.nlm.nih.gov/pubmed/34925207
http://dx.doi.org/10.3389/fneur.2021.734515

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674198/
https://www.ncbi.nlm.nih.gov/pubmed/34925207
http://dx.doi.org/10.3389/fneur.2021.734515

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