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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Veröffentlicht in:Mol Genet Genomic Med
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley and Sons Inc. 2021
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Original Articles
Online Zugang: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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