A never-ending story: the steadily growing family of the FA and FA-like genes
Author:
Affiliation:
1. Équipe labellisée La Ligue contre le Cancer, France; Gustave Roussy Cancer Center, France; Université Paris Saclay, France
2. Universidade Federal do Rio de Janeiro, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v40n2/1415-4757-gmb-1678-4685-GMB-2016-0213.pdf
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2. A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51;Ameziane N;Nat Commun,2015
3. Biallelic inactivation of REV7 is associated with Fanconi anemia;Bluteau D;J Clin Invest,2016
4. Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia;Bogliolo M;Am J Hum Genet,2013
5. Fanconi anemia: A model disease for studies on human genetics and advanced therapeutics;Bogliolo M;Curr Opin Genet Dev,2015
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