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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Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2021
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8222852/
https://ncbi.nlm.nih.gov/pubmed/33825325
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1678
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