Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.

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Published in Hum Mol Genet on October 01, 1999

Authors

A Wilson1, D Leclerc, D S Rosenblatt, R A Gravel

Author Affiliations

1: MRC Group in Medical Genetics, Montreal Children's Hospital, Canada.

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