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Gene polymorphisms associated with diminished activity of 5,10‐methylenetetrahydrofolate reductase do not explain the clinical manifestations of cobalamin deficiency
Author(s) -
Carmel Ralph,
Pullarkat Vinod
Publication year - 2003
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1046/j.1365-2141.2003.04151_1.x
Subject(s) - cobalamin , methylenetetrahydrofolate reductase , medicine , intrinsic factor , allele , cyanocobalamin , pernicious anaemia , endocrinology , methionine synthase , gastroenterology , methionine , biology , genetics , vitamin b12 , gene , amino acid