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Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation

Hereditary hearing loss is characterized by remarkable phenotypic heterogeneity. Patients with the same pathogenic mutations may exhibit various hearing loss phenotypes. In the Chinese population, the c.235delC mutation is the most common pathogenic mutation of GJB2 and is closely related to heredit...

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Detalhes bibliográficos
Publicado no:Neural Plast
Main Authors: Guo, Chang, Huang, Sha-Sha, Yuan, Yong-Yi, Zhou, Ying, Wang, Ning, Kang, Dong-Yang, Yang, Su-Yan, Zhang, Xin, Gao, Xue, Dai, Pu
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7416285/
https://ncbi.nlm.nih.gov/pubmed/32802038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/8841522
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