Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

Overview of attention for article published in Journal of Translational Medicine, November 2013

Altmetric Badge

Mentioned by

twitter: 1 X user

Citations

dimensions_citation: 25 Dimensions

Readers on

mendeley: 21 Mendeley

Summary X Dimensions citations

So far, Altmetric has seen 1 X post from an account with 78 followers.

Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive… http://t.co/6KB6QJKbCH #JTransMed

Reply Repost Favourite

This page shows the most recent X posts that mention this research output.

Click here to find out how to access more activity.