Impaired cotranslational processing as a mechanism for type I antithrombin deficiency. [electronic resource]
Producer: 19990205Description: 4671-6 p. digitalISSN:- 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
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.