Association of X-prolyl aminopeptidase 1 rs17095355 polymorphism with biliary atresia in Thai children

Hepatology Research

Volumn 41, Issue 12, 2011, Pages 1249-1252

  Kaewkiattiyot, Sarannut ^a   Honsawek, Sittisak ^a   Vejchapipat, Paisarn ^a   Chongsrisawat, Voranush ^a   Poovorawan, Yong ^a  

^a CHULALONGKORN UNIVERSITY   (Thailand)

Author keywords

Biliary atresia; Polymorphism; X prolyl aminopeptidase 1 (XPNPEP1)

Indexed keywords

PROLINE IMINOPEPTIDASE; UNCLASSIFIED DRUG; X PROLYL AMINOPEPTIDASE 1;

ADOLESCENT; ARTICLE; BILE DUCT ATRESIA; CHILD; CHILDHOOD DISEASE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE FREQUENCY; GENE SEQUENCE; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; THAILAND;

EID: 82255181542     PISSN: 13866346     EISSN: 1872034X     Source Type: Journal    
DOI: 10.1111/j.1872-034X.2011.00870.x     Document Type: Article

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