Author:
Inal-Gültekin Güldal,Toptaş-Hekimoğlu Bahar,Görmez Zeliha,Gelişin Özlem,Durmuş Hacer,Ergüner Bekir,Demirci Hüseyin,Sağıroğlu Mahmut Ş.,Parman Yeşim,Deymeer Feza,Yılmaz-Aydoğan Hülya,Pençe Sadrettin,Bekircan-Kurt Can Ebru,Tan Ersin,Erdem-Özdamar Sevim,Üstek Duran,Giger Urs,Öztürk Oğuz,Serdaroğlu-Oflazer Piraye
Funder
Scientific Research Projects Coordination Unit of Istanbul University
Republic of Turkey Ministry of Development Infrastructure
Scientific and Technological Research Council of Turkey
Turkish Neurological Society
National Institutes of Health
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference47 articles.
1. Metabolic myopathies: a clinical approach; part II;Darras;Pediatr Neurol,2000
2. Glycogen storage diseases and other inherited disorders of carbohydrate metabolism;Chen,2005
3. Muscle glycogenoses: an overview;DiMauro;Acta Myol,2007
4. McArdle disease: what do neurologists need to know?;Lucia;Nat Clin Pract Neurol,2008
5. A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle disease;Deschauer;Mol Genet Metab,2001
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