Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11-Reference-Cited by-同舟云学术

Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11

Published:2009-10 Issue:4 Volume:85 Page:482-492
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

zur Stadt Udo,Rohr Jan,Seifert Wenke,Koch Florian,Grieve Samantha,Pagel Julia,Strauß Julia,Kasper Brigitte,Nürnberg Gudrun,Becker Christian,Maul-Pavicic Andrea,Beutel Karin,Janka Gritta,Griffiths Gillian,Ehl Stephan,Hennies Hans Christian

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference49 articles.

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5. Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3–22 by homozygosity mapping;Ohadi;Am. J. Hum. Genet.,1999

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