GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana

Overview of attention for article published in Frontiers in Genetics, September 2019

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In the top 25% of all research outputs scored by Altmetric
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twitter: 36 X users

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Summary X Dimensions citations

So far, Altmetric has seen 46 X posts from 36 X users, with an upper bound of 159,598 followers.

RT @FrontGenetics: New Research: GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana: Our study aimed to investi…

21 Dec 2019

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New Research: GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana: Our study aimed to investigate GJB2 (connexin 26) and GJB6 (connexin 30) mutations associated with non-syndromic childhood hearing impairment (HI) as… https://t.c

21 Dec 2019

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GJB2 and GJB6 Mutations in Non-Syndromic Childhood #Hearing Impairment in #Ghana https://t.co/IZpvdABJZB

23 Oct 2019

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RT @WACCBIP_UG: Our @AASciences DELTAS PhD Fellow, @smadadey, has identified a gene mutation specific to a Ghanaian population that may be…

20 Oct 2019

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