Associated Papers
ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.
Pavan M et al.
Bmc Medical Genetics, 2009
Non-P450 aldehyde oxidizing enzymes: the aldehyde dehydrogenase superfamily.
Marchitti SA et al.
Expert Opinion on Drug Metabolism & Toxicology, 2008
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.
Deak KL et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2005
Select a paper to view details