Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophy

Hearing loss (HL) is one of the most common sensory impairments and etiologically and genetically heterogeneous disorders in humans. Muscular dystrophies (MDs) are neuromuscular disorders characterized by progressive degeneration of skeletal muscle accompanied by non-muscular symptoms. Aberrant glyc...

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Veröffentlicht in:PLoS Genet
Hauptverfasser: Morioka, Shigefumi, Sakaguchi, Hirofumi, Mohri, Hiroaki, Taniguchi-Ikeda, Mariko, Kanagawa, Motoi, Suzuki, Toshiaki, Miyagoe-Suzuki, Yuko, Toda, Tatsushi, Saito, Naoaki, Ueyama, Takehiko
Format: Artigo
Sprache:Inglês
Veröffentlicht: Public Library of Science 2020
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7274486/
https://ncbi.nlm.nih.gov/pubmed/32453729
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1008826
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