Condition: Hypermethioninemia due to deficiency of glycine N-methyltransferase


rs864321678 in CNPY3-GNMT;GNMT gene and Hypermethioninemia due to deficiency of glycine N-methyltransferase PMID 11810299 2002 Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism.

PMID 14739680 2003 Glycine N -methyltransferase deficiency: a new patient with a novel mutation.