GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon

This study aimed to investigate GJB2 (connexin 26) and GJB6 (connexin 30) mutations associated with familial non-syndromic childhood hearing impairment (HI) in Cameroon. We selected only families segregating HI, with at least two affected individuals and with strong evidence of non-environmental cau...

Descripción completa

Detalles Bibliográficos
Autores principales: Tingang Wonkam, Edmond, Chimusa, Emile, Noubiap, Jean Jacques, Adadey, Samuel Mawuli, F. Fokouo, Jean Valentin, Wonkam, Ambroise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895965/
https://www.ncbi.nlm.nih.gov/pubmed/31731535
http://dx.doi.org/10.3390/genes10110844

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895965/
https://www.ncbi.nlm.nih.gov/pubmed/31731535
http://dx.doi.org/10.3390/genes10110844

Ejemplares similares