DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
zur Stadt U, Rohr J, Seifert W. , et al.
Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11.
Am J Hum Genet 2009;
85 (04) 482-492
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