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Esophageal cancer as initial presentation of Fanconi anemia in patients with a hypomorphic FANCA variant
Fanconi anemia (FA) is a clinically heterogenous and genetically diverse disease with 22 known complementation groups (FA-A to FA-W), resulting from the inability to repair DNA interstrand cross-links. This rare disorder is characterized by congenital defects, bone marrow failure, and cancer predisp...
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| Yayımlandı: | Cold Spring Harb Mol Case Stud |
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| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Cold Spring Harbor Laboratory Press
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7784490/ https://ncbi.nlm.nih.gov/pubmed/33172906 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/mcs.a005595 |
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