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...

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Detaylı Bibliyografya
Yayımlandı:BMC Med Genet
Asıl Yazarlar: Zareifar, Soheila, Dastsooz, Hassan, Shahriari, Mahdi, Faghihi, Mohammad Ali, Shekarkhar, Golsa, Bordbar, Mohammadreza, Zekavat, Omid Reza, Shakibazad, Nader
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2019
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6617641/
https://ncbi.nlm.nih.gov/pubmed/31288759
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0855-2
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