TY  - GEN
AU  - Nakagawa,Taku
AU  - Mure,Takeo
AU  - Yusoff,Surini
AU  - Ono,Eiichi
AU  - Kusuma Harahap,Indra Sari
AU  - Morikawa,Satoru
AU  - Morioka,Ichiro
AU  - Takeshima,Yasuhiro
AU  - Nishio,Hisahide
AU  - Matsuo,Masafumi
TI  - A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome
SN  - 1883-0498
PY  - 2012///0404
KW  - Child
KW  - Exons
KW  - Female
KW  - Gilbert Disease
KW  - genetics
KW  - Glucuronosyltransferase
KW  - Haplotypes
KW  - Homozygote
KW  - Humans
KW  - Hyperbilirubinemia
KW  - Male
KW  - Mutation
N1  - Publication Type: Case Reports; Journal Article
ER  -