000 01463 a2200457 4500
005 20250513081519.0
264 0 _c19930519
008 199305s 0 0 eng d
022 _a0006-4971
040 _aNLM
_beng
_cNLM
100 1 _aSimsek, S
245 0 0 _aGlanzmann's thrombasthenia caused by homozygosity for a splice defect that leads to deletion of the first coding exon of the glycoprotein IIIa mRNA.
_h[electronic resource]
260 _bBlood
_cApr 1993
300 _a2044-9 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aAmino Acid Sequence
650 0 4 _aAntibodies, Monoclonal
650 0 4 _aBase Sequence
650 0 4 _aBlood Platelets
_xchemistry
650 0 4 _aDNA
_xchemistry
650 0 4 _aDeoxyribonucleases, Type II Site-Specific
650 0 4 _aExons
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aImmunosorbent Techniques
650 0 4 _aMolecular Sequence Data
650 0 4 _aPlatelet Membrane Glycoproteins
_xchemistry
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aRNA Splicing
_xgenetics
650 0 4 _aRNA, Messenger
_xblood
650 0 4 _aThrombasthenia
_xblood
700 1 _aHeyboer, H
700 1 _ade Bruijne-Admiraal, L G
700 1 _aGoldschmeding, R
700 1 _aCuijpers, H T
700 1 _avon dem Borne, A E
773 0 _tBlood
_gvol. 81
_gno. 8
_gp. 2044-9
999 _c8471035
_d8471035