MTR encodes the enzyme 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G.
References for Human MTR peptide (ab23154)
has not yet been referenced specifically in any publications.
Publishing research using ab23154? Please let us know so that we can cite the reference in this datasheet.
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