Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity (medical condition)

A inborn error of metabolism where an inherited deficiency of methylene tetrahydrofolate reductase causes symptoms of ranging severity - from asymptomatic to severe neurological degeneration and premature death. See also Methylene tetrahydrofolate reductase deficiency

Chemwatch
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