000 01384 a2200397 4500
005 20250518045901.0
264 0 _c20200310
008 202003s 0 0 eng d
022 _a1573-742X
024 7 _a10.1007/s11239-019-01911-z
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMoret, A
245 0 0 _aNext generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiency.
_h[electronic resource]
260 _bJournal of thrombosis and thrombolysis
_cNov 2019
300 _a674-678 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aBlood Coagulation Disorders, Inherited
_xgenetics
650 0 4 _aCodon, Nonsense
650 0 4 _aFactor V
_xgenetics
650 0 4 _aFactor V Deficiency
_xgenetics
650 0 4 _aGenetic Variation
650 0 4 _aHigh-Throughput Nucleotide Sequencing
650 0 4 _aHumans
650 0 4 _aMutation
650 0 4 _aPoint Mutation
700 1 _aZúñiga, Ángel
700 1 _aIbáñez, M
700 1 _aCid, A R
700 1 _aHaya, S
700 1 _aFerrando, F
700 1 _aBlanquer, A
700 1 _aCervera, J
700 1 _aBonanad, S
773 0 _tJournal of thrombosis and thrombolysis
_gvol. 48
_gno. 4
_gp. 674-678
856 4 0 _uhttps://doi.org/10.1007/s11239-019-01911-z
_zAvailable from publisher's website
999 _c29863578
_d29863578