Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients

Fanconi anemia (FA) is a severe hereditary disorder with defective DNA damage response and repair. It is characterized by phenotypes including progressive bone marrow failure (BMF), developmental abnormalities, and increased occurrence of leukemia and cancer. Recent studies in mice have suggested th...

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Detaylı Bibliyografya
Asıl Yazarlar: Hira, Asuka, Yabe, Hiromasa, Yoshida, Kenichi, Okuno, Yusuke, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Nakamura, Jun, Kojima, Seiji, Ogawa, Seishi, Matsuo, Keitaro, Takata, Minoru, Yabe, Miharu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Hematology 2013
Konular:
Red Cells, Iron, and Erythropoiesis
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3953058/
https://ncbi.nlm.nih.gov/pubmed/24037726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-06-507962
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