Abstract
![Figure][1] Insight from William Muller In this issue, [Canault et al.][2] report for the first time a point mutation in the RAS guanyl-releasing protein 2 ( RASGRP2 ) gene that results in a severe bleeding defect in humans. The study of inherited platelet disorders has shed light on the
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
