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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Royan Institute (ACECR), Tehran
2016-09-01
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Series: | Cell Journal |
Subjects: | |
Online Access: | http://celljournal.org/web/journal/article/6122/download |