A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss

AIM: Autosomal dominant non‐syndromic hearing loss is a common sensorineural disorder with extremely high genetic heterogeneity. CEA antigen‐related cell adhesion molecule 16(CEACAM16)is a secreted glycoprotein encoded by the CEACAM16 gene. Mutations in CEACAM16 lead to autosomal dominant non‐syndro...

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Detalles Bibliográficos
Autores principales: Zhang, Dejun, Wu, Jie, Yuan, Yongyi, Li, Xiaohong, Gao, Xue, Han, Mingyu, Gao, Song, Huang, Shasha, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314904/
https://www.ncbi.nlm.nih.gov/pubmed/35292975
http://dx.doi.org/10.1111/ahg.12463

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314904/
https://www.ncbi.nlm.nih.gov/pubmed/35292975
http://dx.doi.org/10.1111/ahg.12463

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