Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with Fanconi anaemia
Fanconi anaemia (FA) is a recessive autosomal disease determined by mutations in genes of at least eleven complementation groups, with distinct distributions in different populations. As far as we know, there are no reports regarding the molecular characterisation of the disease in unselected FA pat...
| Main Authors: | Rodriguez, David Enrique Aguilar, Lima, Carmen Silvia Passos, Lourenço, Gustavo Jacob, Figueiredo, Maria Estela, Carneiro, Jorge David Aivazoglu, Tone, Luiz Gonzaga, Llerena Jr., Juan Clinton, Toscano, Raquel Alves, Brandalise, Silvia, Pinto Júnior, Walter, Costa, Fernando Ferreira, Bertuzzo, Carmen Sílvia |
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| Format: | Artigo |
| Language: | English |
| Published: |
Sociedade Brasileira de Genética
2017
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| Subjects: | |
| Online Access: |
http://repositorio.unb.br/handle/10482/26521 |
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