Molecular study of the perforin gene in familial hematological malignancies

Perforin gene (PRF1) mutations have been identified in some patients diagnosed with the familial form of hemophagocytic lymphohistiocytosis (HLH) and in patients with lymphoma. The aim of the present study was to determine whether patients with a familial aggregation of hematological malignancies ha...

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Detalles Bibliográficos
Autores principales: El Abed, Rim, Bourdon, Violaine, Voskoboinik, Ilia, Omri, Halima, Youssef, Yosra Ben, Laatiri, Mohamed Adnene, Huiart, Laetitia, Eisinger, François, Rabayrol, Laetitia, Frenay, Marc, Gesta, Paul, Demange, Liliane, Dreyfus, Hélène, Bonadona, Valérie, Dugast, Catherine, Zattara, Hélène, Faivre, Laurence, Zaier, Monia, Jemni, Saloua Yacoub, Noguchi, Testsuro, Sobol, Hagay, Soua, Zohra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3197553/
https://www.ncbi.nlm.nih.gov/pubmed/21936944
http://dx.doi.org/10.1186/1897-4287-9-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3197553/
https://www.ncbi.nlm.nih.gov/pubmed/21936944
http://dx.doi.org/10.1186/1897-4287-9-9

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