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    • Mitochondrial copy number and D-loop variants in pompe patients 

      Fatemeh Bahreini; Massoud Houshmand; Mohammad Hossein Modaresi; Hassan Tonekaboni; Shahriar Nafssi; Ferdoss Nazari; Seyed Mohammad Akrami (2016-01-01)
      Objective: Pompe disease is a rare neuromuscular genetic disorder and is classifed into two forms of early and late-onset. Over the past two decades, mitochondrial abnormalities have been recognized as an important contributor ...