Inherited disorders in the conversion of methionine to homocysteine
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-009-1146-4
Reference75 articles.
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2. Avila MA, Berasain C, Torres L, et al (2000) Reduced mRNA abundance of the main enzymes involved in methionine metabolism in human liver cirrhosis and hepatocellular carcinoma. J Hepatol 33:907–914. doi: 10.1016/S0168-8278(00)80122-1
3. Barić I, Fumić K, Glenn B, et al (2004) S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism. Proc Nat Acad Sci U S A 101:4234–4239. doi: 10.1073/pnas.0400658101
4. Barić I, Ćuk M, Fumić K, et al (2005) S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy. J Inherit Metab Dis 28:885–902. doi: 10.1007/s10545-005-0192-9
5. Belužić R, Ćuk M, Pavkov T, et al (2006) A single mutation at Tyr143 of human Sadenosylhomocysteine hydrolase renders the enzyme thermosensitive and affects the oxidation state of bound cofactor nicotinamide-adenine dinucleotide. Biochem J 400:245–253. doi: 10.1042/BJ20060749
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