ArticleHuman molecular genetics2018
Bi-allelic mutations in MYL1 cause a severe congenital myopathy.
Gianina Ravenscroft et al.PubMed ↗Full text ↗Publisher ↗
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ArticleHuman molecular genetics2018
Gianina Ravenscroft et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.