Adult onset of primary hemophagocytic syndrome in subjects carrying PRF1 mutations

Author:

Wang Yini,Wang Zhao,Chen Hua,Wang Xiaolin

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Reference5 articles.

1. Gritta EJ, zur Stadt U (2007) Familial and acquired hemophagocytic lymphohistiocytosis. Eur J Pediatr 166:95–109

2. Valentina C, Daniela P, Gillian MG et al (2010) Molecular basis of familial hemophagocytic lymphohistiocytosis. Haematologica 95(4):538–541

3. Trizzino A, zur Stadt U, Ueda I et al (2008) Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. J Med Genet 45(1):15–21

4. Esther M, Luis MA, María G et al (2006) Familial hemophagocytic lymphohistiocytosis in an adult patient homozygous for A91V in the perforin gene, with tuberculosis infection. Haematologica 91:1257–1260

5. Okur H, Balta G, Akarsu N et al (2008) Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations. Leuk Res 32:972–975

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