Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.

D Leclerc; E Campeau; P Goyette; C E Adjalla; B Christensen; M Ross; P Eydoux; D S Rosenblatt; R Rozen; R A Gravel

doi:10.1093/hmg/5.12.1867

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.

Identifier:nobleid.org/w1/20260515/08CF8FDC

Type:Journal Article

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Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.

Identifier:nobleid.org/w1/20260515/08CF8FDC

Type:Journal Article

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