| Title: |
A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome |
| Authors: |
Al-Numair, Nouf, Ramzan, Khushnooda, Alquait, Laila, Alshehri, Meshal, Imtiaz, Faiqa, Owaidah, Tarek |
| Source: |
Blood coagulation and fibrinolysis. 32(5):352-355 |
| Availability: |
http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122529566.0x000001&indx=1&recIds=ETOCvdc_100122529566.0x000001 |
| Database: |
British Library Document Supply Centre Inside Serials & Conference Proceedings |
