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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Bibliografiska uppgifter
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2011
Ämnen:
Research
Länkar: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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