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Investigation of FANCA gene in Fanconi anaemia patients in Iran
BACKGROUND & OBJECTIVES: Fanconi anaemia (FA) is a syndrome with a predisposition to bone marrow failure, congenital anomalies and malignancies. It is characterized by cellular hypersensitivity to cross-linking agents such as mitomycin C (MMC). In the present study, a new approach was selected t...
Autores principales: | Saffar Moghadam, Ali Akbar, Mahjoubi, Frouzandeh, Reisi, Nahid, Vosough, Parvaneh |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859127/ https://www.ncbi.nlm.nih.gov/pubmed/27121516 http://dx.doi.org/10.4103/0971-5916.180206 |
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