Mitochondrial Copy Number and D-Loop Variants in Pompe Patients

Objective: Pompe disease is a rare neuromuscular genetic disorder and is classified into two forms of early and late-onset. Over the past two decades, mitochondrial abnormalities have been recognized as an important contributor to an array of neuromuscular diseases. We therefore aimed to compare...

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Bibliographic Details
Main Authors: Fatemeh Bahreini, Massoud Houshmand, Mohammad Hossein Modaresi, Hassan Tonekaboni, Shahriar Nafissi, Ferdoss Nazarisi, Seyed Mohammad Akrami
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2016-09-01
Series:Cell Journal
Subjects:
Online Access:http://celljournal.org/web/journal/article/6122/download