Impaired cotranslational processing as a mechanism for type I antithrombin deficiency.

Fitches, A C

Impaired cotranslational processing as a mechanism for type I antithrombin deficiency. [electronic resource] - Blood Dec 1998 - 4671-6 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0006-4971


Adult
Amino Acid Substitution--genetics
Animals
Antithrombins--chemistry
COS Cells
Cell-Free System
DNA Mutational Analysis
Dogs
Female
Gene Expression
Glycosylation
Humans
Leucine--genetics
Microsomes--metabolism
Pancreas--metabolism
Point Mutation--genetics
Proline--genetics
Protein Processing, Post-Translational
Protein Sorting Signals--genetics
Transfection