Disease on EC 2.1.1.10 - homocysteine S-methyltransferase
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homocysteine s-methyltransferase deficiency
[N5-methyltetrahydrofolate: homocysteine methyltransferase deficiency]
Hyperglycinemia, Nonketotic
Novel mutations in the P-protein (glycine decarboxylase) gene in patients with glycine encephalopathy (non-ketotic hyperglycinemia).
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