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Cardiac Involvement in Adults With m.3243A>G MELAS Gene Mutation

✍ Scribed by Tom C.G. Vydt; René F.M. de Coo; Osama I.I. Soliman; Folkert J. ten Cate; Robert-Jan M. van Geuns; Wim B. Vletter; Kees Schoonderwoerd; Bianca J.C. van den Bosch; Hubert J.M. Smeets; Marcel L. Geleijnse


Book ID
113443398
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
796 KB
Volume
99
Category
Article
ISSN
0002-9149

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## Abstract The syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke‐like episode (MELAS) is typically associated with a single point mutation in the mitochondrial genome (mtDNA). Because mtDNA is known to have a higher mutation rate than nuclear DNA, we speculate that some pati