Article
Diseases of adenosine triphosphate synthesis in children.
Current opinion in neurology - 1 Apr 2002
Sims Katherine, Holtzman David
Abstract excerpt
There is an expanding understanding of primary genetic oxidative-phosphorylation disorders and the recognition of new multi-system clinical phenotypes in the energy metabolism diseases. Although initially recognized in association with mitochondrial DNA mutations, there is progress in the more laborious identification of nuclear DNA encoded genes relevant to mitochondrial structure and function. More pathogenic...
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