Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families

Hearing loss is one of the most common sensory disorders in newborns and is mostly caused by genetic factors. Autosomal recessive nonsyndromic hearing loss (ARNSHL) is usually characterized as a severe-to-profound congenital sensorineural hearing loss and later can cause various degrees of defect in...

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Detalles Bibliográficos
Autores principales: Bai, Xiaohui, Zhang, Chi, Zhang, Fengguo, Xiao, Yun, Jin, Yu, Wang, Haibo, Xu, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049443/
https://www.ncbi.nlm.nih.gov/pubmed/32149082
http://dx.doi.org/10.1155/2020/1685974

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049443/
https://www.ncbi.nlm.nih.gov/pubmed/32149082
http://dx.doi.org/10.1155/2020/1685974

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