Glutamate carboxypeptidase II: A polymorphism associated with lower levels of serum folate and hyperhomocysteinemia

Human Molecular Genetics

Volumn 9, Issue 19, 2000, Pages 2837-2844

  Devlin, Angela M ^a   Ling, Erh Hsin ^a   Peerson, Janet M ^b   Fernando, Shama ^c   Clarke, Robert ^d   Smith, A David ^c   Halsted, Charles H ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DNA; FOLIC ACID; FOLIC ACID DERIVATIVE; GAMMA GLUTAMYL HYDROLASE; HOMOCYSTEINE; PTEROPTIN;

ALLELE; ANIMAL CELL; ARTICLE; BRUSH BORDER; CARDIOVASCULAR DISEASE; CAUCASIAN; CELL STRAIN; COGNITIVE DEFECT; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; DNA DETERMINATION; DRUG ABSORPTION; ENZYME ACTIVITY; EXON; FOLIC ACID BLOOD LEVEL; FOLIC ACID DEFICIENCY; GENETIC POLYMORPHISM; GENETIC TRANSFECTION; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; HYPERHOMOCYSTEINEMIA; INTESTINE ABSORPTION; MOLECULAR CLONING; MONKEY; NEURAL TUBE DEFECT; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; SPLICEOSOME; VITAMIN INTAKE;

ANIMALIA;

EID: 0034703861     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.19.2837     Document Type: Article

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