Literature DB >> 10649497

Nomenclature of trypsinogen mutations in hereditary pancreatitis.

N Teich1, A Hoffmeister, V Keim.   

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Year:  2000        PMID： 10649497     DOI： 10.1002/(SICI)1098-1004(200002)15:9<197::AID-HUMU9>3.0.CO;2-6

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  2 in total

Review 1.  Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitis.

Authors:  Niels Teich; Jonas Rosendahl; Miklós Tóth; Joachim Mössner; Miklós Sahin-Tóth
Journal:  Hum Mutat       Date:  2006-08       Impact factor: 4.878

2.  Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatography.

Authors:  C Le Maréchal; J M Chen; I Quéré; O Raguénès; C Férec; J Auroux
Journal:  BMC Genet       Date:  2001-11-19       Impact factor: 2.797
  2 in total

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