Glanzmann Thrombasthenia, an exceptional inherited platelet disorder is characterized by a complete lack of platelet aggregation due to a defect in the alpha(IIb)beta(3) complex or to a qualitative abnormality of this complex. Advances in molecular biology have permitted to precise the molecular abn
✦ LIBER ✦
Treatment of spontaneous intracerebral haemorrhage in Glanzmann's thrombasthenia
✍ Scribed by P. Vigren; J. O. Ström; P. Petrini; M. Callander; A. Theodorsson
- Book ID
- 114729076
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 120 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1351-8216
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