000 01349 a2200445 4500
005 20250513105148.0
264 0 _c19961231
008 199612s 0 0 eng d
022 _a0006-4971
040 _aNLM
_beng
_cNLM
100 1 _aSimmonds, R E
245 0 0 _aIdentification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study Group.
_h[electronic resource]
260 _bBlood
_cDec 1996
300 _a4195-204 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlleles
650 0 4 _aAmino Acid Sequence
650 0 4 _aAnimals
650 0 4 _aCattle
650 0 4 _aChromosomes, Human, Pair 3
_xgenetics
650 0 4 _aCodon
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDisease Susceptibility
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMice
650 0 4 _aPedigree
650 0 4 _aPoint Mutation
650 0 4 _aProtein S
_xgenetics
650 0 4 _aProtein S Deficiency
_xcomplications
650 0 4 _aRats
650 0 4 _aSequence Alignment
650 0 4 _aSequence Homology, Amino Acid
650 0 4 _aThrombosis
_xetiology
700 1 _aIreland, H
700 1 _aKunz, G
700 1 _aLane, D A
773 0 _tBlood
_gvol. 88
_gno. 11
_gp. 4195-204
999 _c8936164
_d8936164