Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene.

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Published in Am J Hum Genet on March 01, 1997

Authors

M E Chamberlin1, T Ubagai, S H Mudd, H L Levy, J Y Chou

Author Affiliations

1: Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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