Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with β thalassemia

Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with β thalassemia

Although β thalassemia is considered to be a classic monogenic disease, it is clear that there is considerable clinical variability between patients who inherit identical β globin gene mutations, suggesting that there may be a variety of genetic determinants influencing different clinical phenotypes...

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書目詳細資料
Main Authors:	Vip Viprakasit, Voravarn S. Tanphaichitr, Worrawut Chinchang, Pakarat Sangkla, Mitchell J. Weiss, Douglas R. Higgs
其他作者:	Mahidol University
格式:	Article
出版:	2018
主題:	Biochemistry, Genetics and Molecular Biology Immunology and Microbiology Medicine
在線閱讀:	https://repository.li.mahidol.ac.th/handle/123456789/21192
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!

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