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Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

Zur Stadt, U., Rohr, J., Seifert, W., Koch, F., Grieve, S., Pagel, J., Strauss, J., Kasper, B., Nürnberg, G., Becker, C., Maul-Pavicic, A., Beutel, K., Janka, G., Griffiths, G., Ehl, S. and Hennies, Hans C. (2009) Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11. American Journal of Human Genetics, 85 (4). pp. 482-492. ISSN 1537-6605
Information
URI:
https://eprints.hud.ac.uk/id/eprint/28790
URI:
https://eprints.hud.ac.uk/id/eprint/28790
Title:
Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11
Creators:
Zur Stadt, U., Rohr, J., Seifert, W., Koch, F., Grieve, S., Pagel, J., Strauss, J., Kasper, B., Nürnberg, G., Becker, C., Maul-Pavicic, A., Beutel, K., Janka, G., Griffiths, G., Ehl, S. and Hennies, Hans C.
Identification Number:
https://doi.org/10.1016/j.ajhg.2009.09.005
Official URL:
http://dx.doi.org/10.1016/j.ajhg.2009.09.005
Date:
8 October 2009
Subjects:
Q Science > QH Natural history > QH301 Biology
Q Science > QH Natural history > QH426 Genetics
Schools:
School of Applied Sciences
Additional Information:
Unmapped bibliographic data: ST - Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11 [Field not mapped to EPrints] LB - 93 [Field not mapped to EPrints] RP - Not in File [Field not mapped to EPrints]
Uncontrolled Keywords:
Binding, Infant
Library
Item Type:
Article
Depositing User:
Hans Hennies
Date Deposited:
13 Jul 2016 14:14
Revision:
11
Last Modified:
28 Aug 2021 12:05
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