Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Daniele Vaccaro"'
Autor:
Martina Bartolucci, Cristina Capanni, Marta Columbaro, Daniele Vaccaro, Enrico Cappelli, Isabella Panfoli, Silvia Ravera, Paola Cuccarolo, Alessandro Morelli, Carlo Dufour, Paolo Degan
Fanconi anemia (FA) is a rare and complex inherited blood disorder of the child. At least 15 genes are associated with the disease. The highest frequency of mutations belongs to groups A, C and G. Genetic instability and cytokine hypersensitivity sup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0df6ac2c5953544885327763c9334f4
https://hdl.handle.net/11567/748592
https://hdl.handle.net/11567/748592
Autor:
Martina Bartolucci, Silvia Ravera, Paola Cuccarolo, Carlo Dufour, Isabella Panfoli, Enrico Cappelli, Daniele Vaccaro, Paolo Degan
Publikováno v:
Trends in Molecular Medicine. 19:513-514
Fanconi anemia (FA) is a rare, complex disorder that manifests in childhood. Children with FA suffer bone marrow failure, leukemias, or solid tumors. FA-associated mutations are found in 15 proteins that are involved in DNA repair. Some of these prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec42e282117691fc1eb7b2bfee890c4c
https://doi.org/10.1016/j.molmed.2013.07.008
https://doi.org/10.1016/j.molmed.2013.07.008
