Loading...
Clinical features of MELAS and its relation with A3243G gene point mutation
Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) mostly occur in children. The point mutation A3243G of mitochondrial DNA (mtDNA) may work as a specific bio-marker for mitochondrial disorders. The related clinical features, however, may vary among individuals. This...
Saved in:
| Published in: | Int J Clin Exp Pathol |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
e-Century Publishing Corporation
2015
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4680494/ https://ncbi.nlm.nih.gov/pubmed/26722549 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|