Title : Serum betaine, N,N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism.

Pub. Date : 1993 Nov

PMID : 7694037






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Homocysteine and 5-CH3-tetrahydrofolate (5-CH3-THF) are converted to methionine and THF by the CH3-cobalamin (CH3-Cbl)-dependent enzyme methionine synthase. Methionine Cbl proto-oncogene Homo sapiens
2 In patients with cbl C and cbl D mutations, methionine levels remained low or low-normal at 8.3 to 15.6 mumol/L (normal, 13.3 to 42.7) despite betaine treatment. Methionine Cbl proto-oncogene Homo sapiens
3 In patients with cbl C and cbl D mutations, methionine levels remained low or low-normal at 8.3 to 15.6 mumol/L (normal, 13.3 to 42.7) despite betaine treatment. Methionine Cbl proto-oncogene Homo sapiens