A loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders

scientific article published on 3 December 2008

A loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1136/GUT.2008.151688
P698PubMed publication ID19052022

P50authorAtsushi MasamuneQ57017685
P2093author name stringT Watanabe
Y Takagi
T Shimosegawa
K Satoh
K Kume
S Hamada
M Hirota
A Satoh
K Kikuta
P433issue6
P407language of work or nameEnglishQ1860
P304page(s)820-824
P577publication date2008-12-03
P1433published inGutQ5621669
P1476titleA loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders
P478volume58

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cites work (P2860)
Q37983481Chronic pancreatitis in India and Asia
Q35907078Common Variants in CLDN2 and MORC4 Genes Confer Disease Susceptibility in Patients with Chronic Pancreatitis
Q33933584Functional effect of polymorphisms in the promoter of TNFAIP3 (A20) in acute pancreatitis in the Han Chinese population
Q33843764Genetic Risk in Chronic Pancreatitis: The Trypsin-Dependent Pathway
Q33970780Sequence analysis of the human tyrosylprotein sulfotransferase-2 gene in subjects with chronic pancreatitis
Q37065823Tighter Control by Chymotrypsin C (CTRC) Explains Lack of Association between Human Anionic Trypsinogen and Hereditary Pancreatitis
Q60609692−651C/T promoter polymorphism in the CD14 gene is associated with severity of acute pancreatitis in Japan

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