A Rare Case of Severe Congenital RYR1-Associated Myopathy.
Laforgia N, Capozza M, De Cosmo L, Di Mauro A, Baldassarre ME, Mercadante F, Torella AL, Nigro V, Resta N.
Laforgia N, et al. Among authors: capozza m.
Case Rep Genet. 2018 Aug 1;2018:6184185. doi: 10.1155/2018/6184185. eCollection 2018.
Case Rep Genet. 2018.
PMID: 30155320
Free PMC article.