Familial Hemophagocytic Lymphohistiocytosis due to Mutation of UNC13D Gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-014-0494-x.pdf
Reference10 articles.
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2. Schneider EM, Lorenz I, Müller-Rosenberger M et al (2002) Hemophagocytic lymphohistiocytosis is associated with deficiencies of cellular cytolysis but normal expression of transcripts relevant to killercell- induced apoptosis. Blood 89:4100–4103
3. Ueda I, Kurokawa Y, Koike K et al (2007) Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations. Am J Hematol 82:427–432
4. Henter JI, Horne A, Aricó M et al (2007) Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 48:124–131
5. Sieni E, Cetica V, Santoro A et al (2011) Geno-phenotype study of familial hemophagocytic lymphohistiocytosis type 3. J Med Genet 48:343–352
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