Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine.

Mudd SH, Wagner C, Luka Z, Stabler SP, Allen RH, Schroer R, Wood T, Wang J, Wong LJ
Mol Genet Metab. 2012 105 (2): 228-36

PMID: 22137549 · PMCID: PMC3264801 · DOI:10.1016/j.ymgme.2011.11.006

MeSH Terms (18)

Adolescent Base Sequence DNA, Mitochondrial Exons Female Glycine N-Methyltransferase Humans Infant Liver Male Membrane Proteins Methionine Mitochondrial Diseases Mitochondrial Proteins Molecular Sequence Data Mutation S-Adenosylmethionine Sequence Deletion

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