The genetic basis of Gilbert's syndrome

被引：100

作者：

Sato, H

Adachi, Y

Koiwai, O

机构：

[1] KINKI UNIV,SCH MED,DEPT INTERNAL MED 2,OSAKA,OSAKA 577,JAPAN

[2] AICHI CANC CTR,RES INST,DEPT BIOCHEM,NAGOYA,AICHI,JAPAN

来源：

LANCET | 1996年 / 347卷 / 9001期

关键词：

D O I：

10.1016/S0140-6736(96)91266-0

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：557 / 558

页数：2

共 5 条

[1] ANALYSIS OF GENES FOR BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE IN GILBERTS-SYNDROME [J].

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[2] THE GENETIC-BASIS OF THE REDUCED EXPRESSION OF BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE-1 IN GILBERTS-SYNDROME [J].

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[3] GILBERTS-SYNDROME IS CAUSED BY A HETEROZYGOUS MISSENSE MUTATION IN THE GENE FOR BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE [J].

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SATO, H .

HUMAN MOLECULAR GENETICS, 1995, 4 (07) :1183-1186

[4] GILBERTS-SYNDROME - A LEGITIMATE GENETIC ANOMALY [J].

SCHMID, R .

NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (18) :1217-1218

[5] PREDICTED HOMOZYGOUS MIS-SENSE MUTATION IN GILBERTS-SYNDROME [J].

SOEDA, Y ;

YAMAMOTO, K ;

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HORI, T ;

AONO, S ;

KOIWAI, O ;

SATO, H .

LANCET, 1995, 346 (8988) :1494-1494

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