Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy

February 11, 2019
Nat Commun
https://pubmed.ncbi.nlm.nih.gov/30770808

This article is currently being updated. View its version on PubMed.

https://pubmed.ncbi.nlm.nih.gov/30770808

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