You are here

  • Home
  • Archive
  • Volume 40, Issue 3
  • The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

Citation Tools

Article menu
Download PDFPDF
Short report
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

Download to a citation manager

Download the citation for this article by clicking on one of the following citation managers:

Cite this article as:
Chol M, Lebon S, Bénit P, et al
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
Journal of Medical Genetics 2003;40:188-191.