000 01452 a2200433 4500
005 20250515000521.0
264 0 _c20061108
008 200611s 0 0 eng d
022 _a1351-8216
024 7 _a10.1111/j.1365-2516.2005.01137.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOnland, W
245 0 0 _aCongenital deficiency of factor XIII caused by two missense mutations in a Dutch family.
_h[electronic resource]
260 _bHaemophilia : the official journal of the World Federation of Hemophilia
_cSep 2005
300 _a539-47 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aChild, Preschool
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFactor XIII
_xgenetics
650 0 4 _aFactor XIII Deficiency
_xcongenital
650 0 4 _aFemale
650 0 4 _aHemorrhage
_xetiology
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aMutation, Missense
650 0 4 _aPedigree
650 0 4 _aUmbilical Cord
700 1 _aBöing, A N
700 1 _aMeijer, A B
700 1 _aSchaap, M C L
700 1 _aNieuwland, R
700 1 _aHaasnoot, K
700 1 _aSturk, A
700 1 _aPeters, M
773 0 _tHaemophilia : the official journal of the World Federation of Hemophilia
_gvol. 11
_gno. 5
_gp. 539-47
856 4 0 _uhttps://doi.org/10.1111/j.1365-2516.2005.01137.x
_zAvailable from publisher's website
999 _c15765224
_d15765224