Intermediate hyperhomocysteinaemia and compound heterozygosity for the common variant c.677C>T and a MTHFR gene mutation.

Journal of inherited metabolic disease

Volumn 30, Issue 3, 2007, Pages 401-

  Rummel, T ^a   Suormala, T ^a   Haberle J ^a   Koch, H G ^a   Berning, C ^a   Perrett, D ^a   Fowler, B ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HOMOCYSTEINE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);

ARTICLE; BLOOD; GENETIC VARIABILITY; GENETICS; GENOTYPE; HETEROZYGOTE DETECTION; HUMAN; SINGLE NUCLEOTIDE POLYMORPHISM;

GENOTYPE; HETEROZYGOTE DETECTION; HOMOCYSTEINE; HUMANS; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); POLYMORPHISM, SINGLE NUCLEOTIDE; VARIATION (GENETICS);

EID: 34548038162     PISSN: None     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-007-0445-x     Document Type: Article

References (0)