000 01216 a2200361 4500
005 20250512203500.0
264 0 _c19850308
008 198503s 0 0 eng d
022 _a0390-5748
024 7 _a10.1007/BF02904878
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKluft, C
245 0 0 _aCongenital deficiencies in alpha 2-antiplasmin.
_h[electronic resource]
260 _bLa Ricerca in clinica e in laboratorio
_c
300 _a507-13 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aBinding Sites
650 0 4 _aBlood Coagulation Disorders
_xcongenital
650 0 4 _aFibrin
_xmetabolism
650 0 4 _aFibrinolysin
_xmetabolism
650 0 4 _aFibrinolysis
650 0 4 _aGenetic Carrier Screening
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aLysine
_xmetabolism
650 0 4 _aMethods
650 0 4 _aPlasminogen
_xmetabolism
650 0 4 _aalpha-2-Antiplasmin
_xanalysis
700 1 _aNieuwenhuis, H K
700 1 _aVellenga, E
773 0 _tLa Ricerca in clinica e in laboratorio
_gvol. 14
_gno. 3
_gp. 507-13
856 4 0 _uhttps://doi.org/10.1007/BF02904878
_zAvailable from publisher's website
999 _c6240741
_d6240741