Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

Overview of attention for article published in Genetics in Medicine, September 2018

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So far, Altmetric has seen 9 X posts from 9 X users, with an upper bound of 41,775 followers.

RT @GIMJournal: Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37 @d_shelley #openaccess https://t.co/K7oR3…

RT @TheACMG: Study aimed at determining the genetic cause of autosomal dominant nonsyndromic hearing loss segregating in a multigenerationa…

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