<i>GJB2</i> and <i>GJB6</i> Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon
This study aimed to investigate <i>GJB2</i> (connexin 26) and <i>GJB6</i> (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 st...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2019-10-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/10/11/844 |