Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization

Overview of attention for article published in American Journal of Human Genetics, October 2016

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twitter: 13 X users

patent: 2 patents

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RRIDs were included in the The American Journal of Human Genetics paper "Variants in the Oxidoreductase PYROXD1 Cause Early…" (https://t.co/muLRqMsp5j). Thank you for making your #methodsmatter. #RRID

RT @pgpaed: PhD students' publication @kids_research identify PYROXD1 as a novel genetic cause of infantile myopathy https://t.co/WSr4Ex4c2…

PhD students' publication @kids_research identify PYROXD1 as a novel genetic cause of infantile myopathy https://t.co/WSr4Ex4c2O @syd_health

Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar… https://t.co/qjGPyTVATl

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