Mitochondrial variants in pompe disease: a comparison between classic and non-classic forms
Cell Journal [Yakhteh]. 2018; 20 (3): 333-339
in English
| IMEMR
| ID: emr-197611
ABSTRACT
Objective:
Pompe disease [PD] is a progressive neuromuscular disorder that is caused by glucosidase acid alpha [GAA] deleterious mutations. Mitochondrial involvement is an important contributor to neuromuscular diseases. In this study the sequence of MT-ATP 6/8 and Cytochrome C oxidase I/II genes along with the expression levels of the former genes were compared in classic and non-classic patients
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Index:
IMEMR (Eastern Mediterranean)
Language:
English
Journal:
Cell J. [Yakhteh]
Year:
2018
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