000 01551 a2200409 4500
005 20250515035441.0
264 0 _c20061012
008 200610s 0 0 eng d
022 _a0957-5235
024 7 _a10.1097/01.mbc.0000240927.88177.d1
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRost, Simone
245 0 0 _aFounder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1.
_h[electronic resource]
260 _bBlood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
_cSep 2006
300 _a503-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aCarbon-Carbon Ligases
_xgenetics
650 0 4 _aConserved Sequence
_xgenetics
650 0 4 _aFemale
650 0 4 _aFounder Effect
650 0 4 _aHaplotypes
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMixed Function Oxygenases
_xdeficiency
650 0 4 _aSequence Analysis, DNA
650 0 4 _aVitamin K
_xadministration & dosage
650 0 4 _aVitamin K Epoxide Reductases
700 1 _aGeisen, Christof
700 1 _aFregin, Andreas
700 1 _aSeifried, Erhard
700 1 _aMüller, Clemens R
700 1 _aOldenburg, Johannes
773 0 _tBlood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
_gvol. 17
_gno. 6
_gp. 503-7
856 4 0 _uhttps://doi.org/10.1097/01.mbc.0000240927.88177.d1
_zAvailable from publisher's website
999 _c16493355
_d16493355