Genetic and clinical spectrums in Korean Charcot‐Marie‐Tooth disease patients with myelin protein zero mutations

BACKGROUND: Charcot‐Marie‐Tooth disease (CMT) is the most common disorder of inherited peripheral neuropathies characterized by distal muscle weakness and sensory loss. CMT is usually classified into three types, demyelinating, axonal, and intermediate neuropathies. Mutations in myelin protein zero...

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Detalles Bibliográficos
Autores principales: Kim, Hye Jin, Nam, Soo Hyun, Kwon, Hye Mi, Lim, Si On, Park, Jae Hong, Kim, Hyun Su, Kim, Sang Beom, Lee, Kyung Suk, Lee, Ji Eun, Choi, Byung‐Ok, Chung, Ki Wha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222852/
https://www.ncbi.nlm.nih.gov/pubmed/33825325
http://dx.doi.org/10.1002/mgg3.1678

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222852/
https://www.ncbi.nlm.nih.gov/pubmed/33825325
http://dx.doi.org/10.1002/mgg3.1678

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