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
Metadata only available from this repository.
Official URL: http://dx.doi.org/10.1016/j.ajhg.2009.09.005
Item Type: | Article |
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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 |
Subjects: | Q Science > QH Natural history > QH301 Biology Q Science > QH Natural history > QH426 Genetics |
Schools: | School of Applied Sciences |
Related URLs: | |
Depositing User: | Hans Hennies |
Date Deposited: | 13 Jul 2016 14:14 |
Last Modified: | 28 Aug 2021 12:05 |
URI: | http://eprints.hud.ac.uk/id/eprint/28790 |
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