Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53

Published 2015 View Full Article

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Title
Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53
Authors
Keywords
<em class=EmphasisTypeItalic >COL11A2</em>, Exome sequencing, Hearing loss, Mutation, Structural modeling
Journal
MOLECULAR GENETICS AND GENOMICS
Volume 290, Issue 4, Pages 1327-1334
Publisher
Springer Nature
Online
2015-01-29
DOI
10.1007/s00438-015-0995-9
References
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