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Bays HE, Fitch A, Christensen S, Burridge K, Tondt J
Mutation of mitochondrial DNA G13513A presenting with Leigh syndrome, Wolff-Parkinson-White syndrome and cardiomyopathy
& Callaghan, B
The glucagon-like peptide-1 receptoror not
72%), along with a reduced time needed for HE resolution and length of hospital stay, and no differences in serious adverse events
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