MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.
Gene
; 529(1): 119-24, 2013 Oct 15.
Article
in En
| MEDLINE
| ID: mdl-23933414
Key words
ASD; CHD; Congenital heart diseases; DNA; ECHO; Egyptian children; Hcy; MTHFR; Methylenetetrahydrofolate reductase (MTHFR); PCRRFLP; PDA; Polymorphism; SNP; VSD; atrial septal defect; congenital heart diseases; deoxyribonucleic acid; echocardiography; homocysteine; methylene tetrahydrofolate reductase; patent ductus arteriosus; polymerase chain reactionrestriction fragment length polymorphism; single nucleotide polymorphism; ventricular septal defect
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Polymorphism, Genetic
/
Methylenetetrahydrofolate Reductase (NADPH2)
/
Heart Defects, Congenital
/
Homocysteine
Type of study:
Etiology_studies
/
Observational_studies
/
Risk_factors_studies
Limits:
Child
/
Child, preschool
/
Female
/
Humans
/
Male
Country/Region as subject:
Africa
Language:
En
Journal:
Gene
Year:
2013
Document type:
Article