Fibrinogen Baltimore I: polymerization defect associated with a gamma 292Gly----Val (GGC----GTC) mutation. [electronic resource]
Producer: 19910129Description: 2279-83 p. digitalISSN:- 0006-4971
- Adult
- Amino Acid Sequence
- Base Sequence
- Blood Coagulation Disorders -- genetics
- Chromatography, High Pressure Liquid
- Codon
- Female
- Fibrinogens, Abnormal -- chemistry
- Fibrinopeptide A -- metabolism
- Fibrinopeptide B -- metabolism
- Glycine -- genetics
- Humans
- Molecular Sequence Data
- Mutation
- Polymers
- Serine Endopeptidases -- metabolism
- Valine -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.