Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/8904_2016_543
Reference23 articles.
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3. Barić I, Fowler B (2014) Sulphur amino acids. In: Blau N, Duran M, Gibson KM, Dionisi-Vici C (eds) Physicians guide to the diagnosis, treatment and follow-up of inherited metabolic diseases. Springer, Berlin, pp 33–46
4. Barić I, Fumić K, Glenn B et al (2004) S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism. Proc Natl Acad Sci U S A 101:4234–4239
5. Belužić R, Ćuk M, Pavkov T et al (2006) A single mutation at Tyr143 of human S-adenosylhomocysteine hydrolase renders the enzyme thermosensitive and affects the oxidation state of bound cofactor nicotinamide-adenine dinucleotide. Biochem J 400:245–253
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