Crigler-Najjar syndrome type I in Tunisia may be associated with a founder effect related to the Q357R mutation within the UGT1 gene

被引：9

作者：

Francoual, J

Rivierre, A

Mokrani, C

Khrouf, N

Gottrand, F

Myara, A

Le Bihan, B

Capel, L

Lindenbaum, A

Labrune, P

机构：

[1] Hop Antoine Beclere, APHP, Serv Pediat, F-92141 Clamart, France

[2] Hop Antoine Beclere, APHP, Biochim Lab, Clamart, France

[3] Hop St Joseph, Biochim Lab, F-75674 Paris, France

[4] Hop Jeanne de Flandre, Serv Pediat, Lille, France

[5] Ctr Matern & Neonatol Tunis, El Jebri, Tunisia

来源：

HUMAN MUTATION | 2002年 / 19卷 / 05期

关键词：

D O I：

10.1002/humu.10064

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：570 / 571

页数：2

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