Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice

Journal of Pediatrics

Volumn 165, Issue 1, 2014, Pages

  Maruo, Yoshihiro ^a   Morioka, Yoriko ^a   Fujito, Hiroshi ^b,c   Nakahara, Sayuri ^a   Yanagi, Takahide ^a   Matsui, Katsuyuki ^a   Mori, Asami ^a,c   Sato, Hiroshi ^d   Tukey, Robert H ^e   Takeuchi, Yoshihiro ^a  

^a SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

^b Department of Pediatrics Hanwasumiyoshin General Hospital   (Japan)

^c Hino Hospital   (Japan)

^d NAGOYA BUNRI UNIVERSITY   (Japan)

^e UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE;

ALLELE; ARTICLE; BILIRUBIN BLOOD LEVEL; BREAST FEEDING; BREAST MILK; BREAST MILK JAUNDICE; CONTROLLED STUDY; FEMALE; GENE; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INFANT; JAPANESE (PEOPLE); JAUNDICE; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ASIAN CONTINENTAL ANCESTRY GROUP; BILIRUBIN; FEMALE; GENETIC VARIATION; GENOTYPE; GLUCURONOSYLTRANSFERASE; HUMANS; HYPERBILIRUBINEMIA, NEONATAL; INFANT, NEWBORN; JAUNDICE, NEONATAL; MALE; MILK, HUMAN; POLYMERASE CHAIN REACTION;

EID: 84903385410     PISSN: 00223476     EISSN: 10976833     Source Type: Journal    
DOI: 10.1016/j.jpeds.2014.01.060     Document Type: Article

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