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
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F. Schmitz | J. Schnekenburger | W. Domschke | P. Felderbauer | K. Bulut | W. Schmidt | V. Schick | M. Parry | R. Lebert | T. Meister