Author:
Xie Shu-Yang,Li Wei,Ren Zhao-Rui,Huang Shu-Zhen,Zeng Fanyi,Zeng Yi-Tao
Publisher
Springer Science and Business Media LLC
Reference26 articles.
1. Weatherall DJ, Clegg JB. The thalassemia syndromes. Oxford: Blackwell Scientific; 2001.
2. Forget BG. Molecular mechanisms of beta thalassemia. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Disorders of hemoglobin: genetics, pathophysiology, and clinical management. Cambridge: Cambridge University Press; 2001. p. 252–76.
3. Cheng TC, Orkin SH, Antonarakis SE, Potter MJ, Sexton JP, Markham AF, et al. β-Thalassemia in Chinese: use of in vitro RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defects. Proc Natl Acad Sci USA. 1984;81:2821–5.
4. Zeng YT, Huang SZ. Disorders of haemoglobin in China. J Med Genet. 1987;24:578–83.
5. Huang SZ, Zeng FY, Ren ZR, Lu ZH, Rodgers GP, Schechter AN, et al. RNA transcripts of the β-thalassaemia allele IVS-2-654 C-T: a small amount of normally processed bglobin mRNA is still produced from the mutant gene. Br J Haematol. 1994;88:541–6.
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