Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis

被引:14
作者
Chen, JM [1 ]
Mercier, B [1 ]
Ferec, C [1 ]
机构
[1] Univ Hosp, ETSBO, Ctr Biogenet, F-29275 Brest, France
关键词
D O I
10.1136/gut.45.6.916
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
引用
收藏
页码:916 / 916
页数:1
相关论文
共 8 条
[1]  
Cotton RGH, 1998, HUM MUTAT, V12, P1, DOI 10.1002/(SICI)1098-1004(1998)12:1<1::AID-HUMU1>3.0.CO
[2]  
2-M
[3]  
Férec C, 1999, J MED GENET, V36, P228
[4]   Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis [J].
Gorry, MC ;
Gabbaizedeh, D ;
Furey, W ;
Gates, LK ;
Preston, RA ;
Aston, CE ;
Zhang, YZ ;
Ulrich, C ;
Ehrlich, GD ;
Whitcomb, DC .
GASTROENTEROLOGY, 1997, 113 (04) :1063-1068
[5]  
NISHIMORI, 1999, GUT, V44, P259
[6]   Screening for mutations of the cationic trypsinogen gene:: are they of relevance in chronic alcoholic pancreatitis? [J].
Teich, N ;
Mössner, J ;
Keim, V .
GUT, 1999, 44 (03) :413-416
[7]  
Whitcomb David C., 1999, Pancreas, V18, P1, DOI 10.1097/00006676-199901000-00001
[8]   Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene [J].
Whitcomb, DC ;
Gorry, MC ;
Preston, RA ;
Furey, W ;
Sossenheimer, MJ ;
Ulrich, CD ;
Martin, SP ;
Gates, LK ;
Amann, ST ;
Toskes, PP ;
Liddle, R ;
McGrath, K ;
Uomo, G ;
Post, JC ;
Ehrlich, GD .
NATURE GENETICS, 1996, 14 (02) :141-145