Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults

Overview of attention for article published in JAMA Neurology, January 2018

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In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (85th percentile)

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RT @taylorlabncl: A follow up to our 2018 @JAMANeuro paper funded by @4Lilyfoundation describing #mito disease patients with RTN4IP1 varian…

A follow up to our 2018 @JAMANeuro paper funded by @4Lilyfoundation describing #mito disease patients with RTN4IP1 variants (https://t.co/5JzuYA6pzv ). Now we show that both these newly identified RTN4IP1 functions are disrupted in #mito disease

https://t.co/vTq3YhIarZ

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