A rare FANCA gene variation as a breast cancer susceptibility allele in an Iranian population

Fanconi Anemia (FA) is an autosomal recessive syndrome characterized by congenital abnormalities, progressive bone marrow failure and Fanconi anemia complementation group A (FANCA) is also a potential breast and ovarian cancer susceptibility gene. A novel allele with tandem duplication of 13 base pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Abbasi, Sakineh, Rasouli, Mina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436159/
https://www.ncbi.nlm.nih.gov/pubmed/28440412
http://dx.doi.org/10.3892/mmr.2017.6489

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436159/
https://www.ncbi.nlm.nih.gov/pubmed/28440412
http://dx.doi.org/10.3892/mmr.2017.6489

Ejemplares similares