Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy

Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy

Mutation of mitochondrial DNA (mtDNA) G13513A, encoding the ND5 subunit of respiratory chain complex I, can cause mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and Leigh syndrome. Wolff-Parkinson-White (WPW) syndrome and optic atrophy were reported in a high prop...

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Bibliographic Details
Main Authors: Shi-Bing Wang, Wen-Chin Weng, Ni-Chung Lee, Wuh-Liang Hwu, Pi-Chuan Fan, Wang-Tso Lee
Format: Article
Language:English
Published: Elsevier 2008-08-01
Series:Pediatrics and Neonatology
Subjects:
cardiomyopathy
electron transfer complex I
Leigh syndrome
Wolff-Parkinson-White syndrome
Online Access:http://www.sciencedirect.com/science/article/pii/S1875957208600303
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