Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier

Overview of attention for article published in Brain, June 2014

Altmetric Badge

About this Attention Score

In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (86th percentile)
Above-average Attention Score compared to outputs of the same age and source (60th percentile)

Mentioned by

twitter: 3 X users

patent: 5 patents

Readers on

mendeley: 68 Mendeley

So far, Altmetric has seen 3 X posts from 3 X users, with an upper bound of 79,157 followers.

Deep intronic OPA1 mutations explain several previously unsolved cases of optic neuropathy. http://t.co/RppbmxDGZh http://t.co/lW17Z7NSGL

Deep intronic OPA1 mutations explain several previously unsolved cases of optic neuropathy. http://t.co/RppbmxDGZh http://t.co/lW17Z7NSGL

Deep intronic OPA1 mutations explain several previously unsolved cases of optic neuropathy. http://t.co/RppbmxDGZh http://t.co/lW17Z7NSGL

This page shows the most recent X posts that mention this research output. Click here to find out how to access more activity.

Login to access the Sentiment Analysis related to this output.