Mitochondrial copy number and d-loop variants in Pompe patients
Cell Journal [Yakhteh]. 2016; 18 (3): 405-415
in English
| IMEMR
| ID: emr-183776
ABSTRACT
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 mitochondrial copy number and mitochondrial displacement-loop sequence variation in infantile and adult Pompe patients
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Index:
IMEMR (Eastern Mediterranean)
Language:
English
Journal:
Cell J. [Yakhteh]
Year:
2016
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