Relationships of mRNA-protein secondary structures in the human β-globin gene HBB and four variants

Author:

Li YanFei,Ye DongHai,Zhang Wen,Wang ChuanMing,Liu CiQuan,Cao Huai

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference32 articles.

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2. Wiwanitkit V. Analysis of functional aberration of some important beta hemoglobinopathies (hemoglobin C, D, E and S) from nanostructures. Nanomedicine, 2005, 1: 213–215

3. Pauling L, Itano H, Singer S J, et al. Sickle cell anemia, a molecular disease. Science, 1949, 110: 543–548

4. Schnog J B, Duits A J, Muskiet F A, et al. Sickle cell disease: A general overview. Neth J Med, 2004, 62: 364–374

5. Orkin S H, Kazazian Jr H H, Antonarakis S E, et al. Abnormal RNA processing due to exon mutation of the β E-globin gene. Nature, 1982, 300: 768–769

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