Biallelic Variants in TTLL5, Encoding a Tubulin Glutamylase, Cause Retinal Dystrophy

Overview of attention for article published in American Journal of Human Genetics, May 2014

Altmetric Badge

About this Attention Score

So far, Altmetric has seen 6 X posts from 6 X users, with an upper bound of 124,079 followers.

New! @VincentPlagnol & colleagues find TTLL5 mutations in retinal dystrophy in a gene-based case:control study. http://t.co/rGSei5wrjG

New! @VincentPlagnol & colleagues find TTLL5 mutations in retinal dystrophy in a gene-based case:control study. http://t.co/rGSei5wrjG

New! @VincentPlagnol & colleagues find TTLL5 mutations in retinal dystrophy in a gene-based case:control study. http://t.co/rGSei5wrjG

New! @VincentPlagnol & colleagues find TTLL5 mutations in retinal dystrophy in a gene-based case:control study. http://t.co/rGSei5wrjG

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

Click here to find out how to access more activity, including 2 additional X posts.