000 01405 a2200373 4500
005 20250516045910.0
264 0 _c20120502
008 201205s 0 0 eng d
022 _a1365-2516
024 7 _a10.1111/j.1365-2516.2011.02621.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aParaboschi, E M
245 0 0 _aFunctional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency.
_h[electronic resource]
260 _bHaemophilia : the official journal of the World Federation of Hemophilia
_cMar 2012
300 _a205-10 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aFactor V
_xgenetics
650 0 4 _aFactor V Deficiency
_xgenetics
650 0 4 _aFrameshift Mutation
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMutation, Missense
_xgenetics
650 0 4 _aSequence Analysis, DNA
700 1 _aKayiran, S M
700 1 _aÖzbek, N
700 1 _aGürakan, B
700 1 _aPeyvandi, F
700 1 _aGuella, I
700 1 _aDuga, S
700 1 _aAsselta, R
773 0 _tHaemophilia : the official journal of the World Federation of Hemophilia
_gvol. 18
_gno. 2
_gp. 205-10
856 4 0 _uhttps://doi.org/10.1111/j.1365-2516.2011.02621.x
_zAvailable from publisher's website
999 _c21024351
_d21024351