P.107Clinical changes over time in patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study

Autor:	C. Lilien, Nicol C. Voermans, A. Grangé, Teresa Gidaro, L. Servais, V. Chê, Andreea Mihaela Seferian, Jonathan Baets, Anthony Behin, W. De Ridder, M. Annoussamy, C. Freitag, L. Thielemans, Marc Bitoun, K. Paradis, J.Y. Hogrel, S. Van Rooijen, D. Duchene
Rok vydání:	2019
Předmět:	medicine.medical_specialty business.industry medicine.disease DNM2 Neurology Internal medicine Pediatrics Perinatology and Child Health medicine In patient Neurology (clinical) Centronuclear myopathy business Gene Genetics (clinical) Natural history study
Zdroj:	Neuromuscular Disorders. 29:S79-S80
ISSN:	0960-8966
DOI:	10.1016/j.nmd.2019.06.163
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::6c53e0d9e9ca7fce26a8f80152bea9b2 https://doi.org/10.1016/j.nmd.2019.06.163 Zobrazit plný text záznamu Full Text from ScienceDirect