A novel A121T mutation in human cationic trypsinogen associated with hereditary pancreatitis: functional data indicating a loss-of-function mutation influencing the R122 trypsin cleavage site

Authors :: Felderbauer, P.
Schnekenburger, J.
Lebert, R.
Bulut, K.
Parry, M.
Meister, T.
Schick, V.
Schmitz, F.
Domschke, W.
Schmidt, W.E.
Source :: Journal of Medical Genetics. August, 2008, Vol. 45 Issue 8, p507, 6 p.
Publication Year :: 2008

Subjects :: Trypsinogen -- Genetic aspects
Trypsinogen -- Research
Pancreatitis -- Genetic aspects
Pancreatitis -- Research
Cleavage (Embryology) -- Analysis
Gene mutations -- Analysis
Health

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