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- W1976230839 abstract "![Figure][1] Insight from William MullerIn 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" @default.
- W1976230839 created "2016-06-24" @default.
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- W1976230839 date "2014-06-30" @default.
- W1976230839 modified "2023-09-25" @default.
- W1976230839 title "Identification of a severe bleeding disorder in humans caused by a mutation in CalDAG-GEFI" @default.
- W1976230839 cites W2057368256 @default.
- W1976230839 doi "https://doi.org/10.1084/jem.2117insight1" @default.
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