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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JAMA Neurology, 03 Feb 2018

RTN4IP1 is a candidate gene to consider in syndromes involving mainly central nervous system features and mitochondrial…

JAMA Neurology, 11 Dec 2017

This case series describes the RTN4IP1 mutations found in 12 children and young adults with severe central nervous system…

Neuroscience Library/Bibliothèque des Neurosciences, 03 Dec 2017

This case series describes the RTN4IP1 mutations found in 12 children and young adults with severe central nervous system…

JAMA Neurology, 29 Nov 2017

RTN4IP1 is a candidate gene to consider in syndromes involving mainly central nervous system features and mitochondrial…

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