Simmonds, R E <br/><br/>
Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study Group.  [electronic resource] 

 -  Blood  Dec 1996 
 - 4195-204 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Animals<br/>Cattle<br/>Chromosomes, Human, Pair 3--genetics<br/>Codon--genetics<br/>DNA Mutational Analysis<br/>Disease Susceptibility<br/>Female<br/>Humans<br/>Male<br/>Mice<br/>Pedigree<br/>Point Mutation<br/>Protein S--genetics<br/>Protein S Deficiency--complications<br/>Rats<br/>Sequence Alignment<br/>Sequence Homology, Amino Acid<br/>Thrombosis--etiology