Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains

Autosomal dominant hearing loss (ADHL) manifests as an adult-onset disease or a progressive disease. MYO7A variants are associated with DFNA11, a subtype of ADHL. Here, we examined the role and genotype–phenotype correlation of MYO7A in ADHL. Enrolled families suspected of having post-lingual sensor...

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Detalles Bibliográficos
Autores principales: Joo, Sun Young, Na, Gina, Kim, Jung Ah, Yoo, Jee Eun, Kim, Da Hye, Kim, Se Jin, Jang, Seung Hyun, Yu, Seyoung, Kim, Hye-Youn, Choi, Jae Young, Gee, Heon Yung, Jung, Jinsei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028242/
https://www.ncbi.nlm.nih.gov/pubmed/35453549
http://dx.doi.org/10.3390/biomedicines10040798

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028242/
https://www.ncbi.nlm.nih.gov/pubmed/35453549
http://dx.doi.org/10.3390/biomedicines10040798

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