A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report

BACKGROUND: Fanconi anemia (FA) is a heterogeneous genetic disorder characterized by congenital anomalies, early-onset bone marrow failure, and a high predisposition to cancers. Up to know, different genes involved in the DNA repair pathway, mainly FANCA genes, have been identified to be affected in...

Descripción completa

Detalles Bibliográficos
Autores principales: Zareifar, Soheila, Dastsooz, Hassan, Shahriari, Mahdi, Faghihi, Mohammad Ali, Shekarkhar, Golsa, Bordbar, Mohammadreza, Zekavat, Omid Reza, Shakibazad, Nader
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617641/
https://www.ncbi.nlm.nih.gov/pubmed/31288759
http://dx.doi.org/10.1186/s12881-019-0855-2

Ejemplares similares

Ejemplares similares