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

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https://eprints.hud.ac.uk/id/eprint/28790

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https://eprints.hud.ac.uk/id/eprint/28790

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https://eprints.hud.ac.uk/id/eprint/28790

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https://eprints.hud.ac.uk/id/eprint/28790

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https://eprints.hud.ac.uk/id/eprint/28790

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https://eprints.hud.ac.uk/id/eprint/28790

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https://eprints.hud.ac.uk/id/eprint/28790

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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:

Identification Number:

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

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Item Type:

Article

Depositing User:

Hans Hennies

Date Deposited:

13 Jul 2016 14:14

Revision:

Last Modified:

28 Aug 2021 12:05