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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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Bibliografski detalji
Izdano u:PLoS Genet
Glavni autori: Morioka, Shigefumi, Sakaguchi, Hirofumi, Mohri, Hiroaki, Taniguchi-Ikeda, Mariko, Kanagawa, Motoi, Suzuki, Toshiaki, Miyagoe-Suzuki, Yuko, Toda, Tatsushi, Saito, Naoaki, Ueyama, Takehiko
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2020
Teme:
Online pristup: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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