S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism.

Baric I, Fumic K, Glenn B, Cuk M, Schulze A, Finkelstein JD, James SJ, Mejaski-Bosnjak V, Pazanin L, Pogribny IP, Rados M, Sarnavka V, Scukanec-Spoljar M, Allen RH, Stabler S, Uzelac L, Vugrek O, Wagner C, Zeisel S, Mudd SH
Proc Natl Acad Sci U S A. 2004 101 (12): 4234-9

PMID: 15024124 · PMCID: PMC384724 · DOI:10.1073/pnas.0400658101

MeSH Terms (12)

Adenosylhomocysteinase Brain Genetic Diseases, Inborn Humans Infant Infant, Newborn Liver Magnetic Resonance Imaging Male Methionine Radiography Ultrasonography

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