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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...

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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

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