Novel PTPRQ variants associated with hearing loss in a Chinese family PTPRQ variants in Chinese hearing loss

IntroductionHearing loss is one of the most prevalent congenital sensory disorders. Over 50% of congenital hearing loss cases are attributed to genetic factors. The PTPRQ gene encodes the protein tyrosine phosphatase receptor Q, which plays an important role in maintaining the structure and function...

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Principais autores:	Yuan Hou, Yuanzhen Shi, Longyan Liu, Shihong Duan
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Frontiers Media S.A. 2024-08-01
Colecção:	Frontiers in Genetics
Assuntos:	protein tyrosine phosphatase receptor Q Non-syndromic hearing loss hereditary disease PTPRQ next-generation sequencing
Acesso em linha:	https://www.frontiersin.org/articles/10.3389/fgene.2024.1399760/full
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