Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele.

Birth defects research. Part A, Clinical and molecular teratology

Volumn 88, Issue 8, 2010, Pages 689-694

  O'Byrne, Michelle R ^a   Au, Kit Sing ^b   Morrison, Alanna C ^b   Lin, Jone Ing ^b   Fletcher, Jack M ^b   Ostermaier, Kathryn K ^b   Tyerman, Gayle H ^b   Doebel, Sabine ^b   Northrup, Hope ^b  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; FOLATE RECEPTOR 1; FOLATE RECEPTOR 2; FOLR3 PROTEIN, HUMAN; REDUCED FOLATE CARRIER; SLC19A1 PROTEIN, HUMAN;

ADOLESCENT; ADULT; ARTICLE; CAUCASIAN; CHILD; COHORT ANALYSIS; FEMALE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETICS; HISPANIC; HUMAN; INFANT; MALE; MENINGOMYELOCELE; MIDDLE AGED; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADULT; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; FOLATE RECEPTOR 1; FOLATE RECEPTOR 2; GENETIC ASSOCIATION STUDIES; GENETIC LINKAGE; HISPANIC AMERICANS; HUMANS; INFANT; MALE; MENINGOMYELOCELE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; REDUCED FOLATE CARRIER PROTEIN; YOUNG ADULT;

EID: 79952112404     PISSN: None     EISSN: 15420760     Source Type: Journal    
DOI: 10.1002/bdra.20706     Document Type: Article

References (0)