Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study Group. [electronic resource]
Producer: 19961231Description: 4195-204 p. digitalISSN:- 0006-4971
- Alleles
- Amino Acid Sequence
- Animals
- Cattle
- Chromosomes, Human, Pair 3 -- genetics
- Codon -- genetics
- DNA Mutational Analysis
- Disease Susceptibility
- Female
- Humans
- Male
- Mice
- Pedigree
- Point Mutation
- Protein S -- genetics
- Protein S Deficiency -- complications
- Rats
- Sequence Alignment
- Sequence Homology, Amino Acid
- Thrombosis -- etiology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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