NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules-Reference-Cited by-同舟云学术

NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules

Published:2011-07-17 Issue:8 Volume:43 Page:732-734
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Gunay-Aygun Meral,Falik-Zaccai Tzipora C,Vilboux Thierry,Zivony-Elboum Yifat,Gumruk Fatma,Cetin Mualla,Khayat Morad,Boerkoel Cornelius F,Kfir Nehama,Huang Yan,Maynard Dawn,Dorward Heidi,Berger Katherine,Kleta Robert,Anikster Yair,Arat Mutlu,Freiberg Andrew S,Kehrel Beate E,Jurk Kerstin,Cruz Pedro,Mullikin Jim C,White James G,Huizing Marjan,Gahl William A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.883.pdf

Reference15 articles.

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3. Weiss, H.J. et al. Blood 54, 1296–1319 (1979).

4. Gunay-Aygun, M., Huizing, M. & Gahl, W.A. Semin. Thromb. Hemost. 30, 537–547 (2004).

5. Nurden, A.T. & Nurden, P. Blood Rev. 21, 21–36 (2007).

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