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Fanconi anemia-D1 due to homozygosity for the BRCA2 gene Cypriot founder mutation: A case report
Fanconi anemia (FA) is a rare disorder characterized by multiple congenital malformations, progressive bone marrow failure and susceptibility to malignancies. Biallelic mutations in the breast cancer 2, early onset (BRCA2) gene are responsible for the FA-D1 subgroup, which accounts for ~3% of all th...
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| Udgivet i: | Oncol Lett |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
D.A. Spandidos
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4727152/ https://ncbi.nlm.nih.gov/pubmed/26834852 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2015.3852 |
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