Myophosphorylase (PYGM) mutations in Turkish patients with McArdle disease: A next generation sequencing study

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Bibliographic Details
Published in:	Neuromuscular disorders : NMD Vol. 25; p. S220
Main Authors:	Inal Gültekin, G, Toptaş Hekimoğlu, B, Görmez, Z, Durmuş, H, Demirci, H, Sağıroğlu, M, Parman, Y, Deymeer, F, Yılmaz, H, Pençe, S, Kurt, C, Tan, E, Özdamar, S, Giger, U, Öztürk, O, Serdaroğlu-Oflazer, P
Format:	Journal Article
Language:	English
Published:	01-10-2015
Subjects:	Neurology
Online Access:	Get full text
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