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A novel fusion gene and a common α0-thalassemia deletion cause hemoglobin H disease in a Chinese family

✍ Scribed by Huang, Ji-Wei; Shang, Xuan; Zhao, Ying; Cai, Ren; Zhang, Xin-Hua; Wei, Xiao-Feng; Xiong, Fu; Xu, Xiang-Min


Book ID
120187615
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
450 KB
Volume
51
Category
Article
ISSN
1079-9796

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