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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3197553/
https://ncbi.nlm.nih.gov/pubmed/21936944
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1897-4287-9-9
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