Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease.


Inal-Gültekin G., Toptaş-Hekimoğlu B., Görmez Z., Gelişin Ö., Durmuş H., Ergüner B., ...More

Neuromuscular disorders : NMD, vol.27, pp.997-1008, 2017 (Peer-Reviewed Journal) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 27
  • Publication Date: 2017
  • Doi Number: 10.1016/j.nmd.2017.06.004
  • Journal Name: Neuromuscular disorders : NMD
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.997-1008