GFI1B mutation causes a bleeding disorder with abnormal platelet function-Reference-Cited by-同舟云学术

GFI1B mutation causes a bleeding disorder with abnormal platelet function

Published:2013-11 Issue:11 Volume:11 Page:2039-2047
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Stevenson W. S.¹²,Morel-Kopp M.-C.¹²,Chen Q.¹²,Liang H. P.²,Bromhead C. J.³,Wright S.²,Turakulov R.⁴,Ng A. P.⁵⁶,Roberts A. W.⁵⁷,Bahlo M.³⁸,Ward C. M.¹²

Affiliation:

1. Department of Haematology; Royal North Shore Hospital; Sydney NSW Australia

2. Northern Blood Research Centre; Kolling Institute of Medical Research; The University of Sydney; Sydney NSW Australia

3. Bioinformatics Division; The Walter and Eliza Hall Institute of Medical Research; Melbourne Victoria Australia

4. Australian Genome Research Facility; Melbourne Victoria Australia

5. Cancer and Haematology Division; The Walter and Eliza Hall Institute of Medical Research; Melbourne Victoria Australia

6. Department of Medical Biology; The University of Melbourne; Melbourne Victoria Australia

7. Department of Medicine; The University of Melbourne; Melbourne Victoria Australia

8. Department of Mathematics and Statistics; The University of Melbourne; Melbourne Victoria Australia

Funder

IRIISS

ARC

Cure Cancer Australia/Leukaemia Foundation of Australia

Cancer Council Victoria

Victorian State Government Operational Infrastructure Support

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12368/fullpdf

Reference29 articles.

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3. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Hegglin/Fechtner Syndrome Consortium;Seri;Nat Genet,2000

4. NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules;Gunay-Aygun;Nat Genet,2011

5. Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1;Nichols;Nat Genet,2000

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