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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Sparad:
Bibliografiska uppgifter
I publikationen:Genes (Basel)
Huvudupphovsmän: Tingang Wonkam, Edmond, Chimusa, Emile, Noubiap, Jean Jacques, Adadey, Samuel Mawuli, F. Fokouo, Jean Valentin, Wonkam, Ambroise
Materialtyp: Artigo
Språk:Inglês
Publicerad: MDPI 2019
Ämnen:
Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6895965/
https://ncbi.nlm.nih.gov/pubmed/31731535
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10110844
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