Nomenclature of trypsinogen mutations in hereditary pancreatitis.
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Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitisDiscrimination 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 chromatographyMutational screening of patients with nonalcoholic chronic pancreatitis: identification of further trypsinogen variants.
P2860
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
description
2000 nî lūn-bûn
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name
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
@en
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
@nl
type
label
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
@en
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
@nl
prefLabel
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
@en
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
@nl
P2093
P2860
P1433
P1476
Nomenclature of trypsinogen mutations in hereditary pancreatitis.
@en
P2093
P2860
P304
P356
10.1002/(SICI)1098-1004(200002)15:9<197::AID-HUMU9>3.0.CO;2-6
P577
2000-01-01T00:00:00Z