Methylenetetrahydrofolate reductase 677C > T mutation and epilepsy

Journal of Inherited Metabolic Disease

Volumn 23, Issue 5, 2000, Pages 525-526

  Ono, H ^a   Sakamoto, A ^a   Mizoguchi, N ^a   Sakura, N ^a  

^a HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); DNA; ENDONUCLEASE; FOLIC ACID; HOMOCYSTEINE; METHIONINE;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CONTROLLED STUDY; DISEASE ASSOCIATION; ENZYME ACTIVITY; EPILEPSY; GENE MUTATION; GENOTYPE; HOMOZYGOSITY; HUMAN; HYPERHOMOCYSTEINEMIA; JAPAN; LEUKOCYTE; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION;

ADOLESCENT; ADULT; ALLELES; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; EPILEPSY; GENE FREQUENCY; GENOTYPE; HUMANS; INFANT; JAPAN; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; POINT MUTATION;

EID: 0033930737     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005680701884     Document Type: Article

References (2)

1. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
2. Molecular genetics of methylenetetrahydrofolate reductase deficiency