UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis

被引：61

作者：

Iolascon, A ^{[1
]}

Faienza, MF

Moretti, A

Perrotta, S

del Giudice, EM

机构：

[1] Univ Bari, Dipartimento Biomedicina Eta Evolut, Bari, Italy

[2] Univ Naples 2, Dipartimento Pediat, Naples, Italy

来源：

BLOOD | 1998年 / 91卷 / 03期

关键词：

D O I：

10.1182/blood.V91.3.1093

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

收藏

页码：1093 / 1093

页数：1

相关论文

共 5 条

[1] THE GENETIC-BASIS OF THE REDUCED EXPRESSION OF BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE-1 IN GILBERTS-SYNDROME
BOSMA, PJ
CHOWDHURY, JR
BAKKER, C
GANTLA, S
DEBOER, A
OOSTRA, BA
LINDHOUT, D
TYTGAT, GNJ
JANSEN, PLM
ELFERINK, RPJO
CHOWDHURY, NR
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (18) : 1171 - 1175
[2] Lux SE., 1995, Blood, P1701
[3] Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
Monaghan, G
Ryan, M
Seddon, R
Hume, R
Burchell, B
[J]. LANCET, 1996, 347 (9001) : 578 - 581
[4] PERROTTA S, 1993, BLOOD, V82, pA459
[5] PINTO L, 1995, INT J PEDIAT HEM ONC, V2, P43