Open AccessDetection of Common Disease-Causing Mutations in Mitochondrial DNA (Mitochondrial Encephalomyopathy, Lactic Acidosis with Stroke-Like Episodes MTTL1 3243 A>G and Myoclonic Epilepsy Associated with Ragged-Red Fibers MTTK 8344A>G) by Real-Time Polymerase Chain Reaction
Author(s) -
Hongxin Fan,
Chris Civalier,
Jessica K. Booker,
Margaret L. Gulley,
Thomas W. Prior,
Rosann A. Farber
Publication year - 2006
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/d20h-rx39
Subject(s) - lactic acidosis , mitochondrial encephalomyopathy , mitochondrial dna , myoclonic epilepsy , epilepsy , mitochondrial disease , medicine , genetics , chemistry , biology , gene , psychiatry
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