Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Thalassemia and HBBP1[original query] |
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A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.
Human genetics 2010 Mar 127 (3): 303-14. Nuinoon Manit, Makarasara Wattanan, Mushiroda Taisei, Setianingsih Iswari, Wahidiyat Pustika Amalia, Sripichai Orapan, Kumasaka Natsuhiko, Takahashi Atsushi, Svasti Saovaros, Munkongdee Thongperm, Mahasirimongkol Surakameth, Peerapittayamongkol Chayanon, Viprakasit Vip, Kamatani Naoyuki, Winichagoon Pranee, Kubo Michiaki, Nakamura Yusuke, Fucharoen Suth |
A single nucleotide polymorphism in the HBBP1 gene in the human ß-globin locus is associated with a mild ß-thalassemia disease phenotype. Hemoglobin 2012 36 (5): 433-45. Giannopoulou Emily, Bartsakoulia Marina, Tafrali Christina, Kourakli Alexandra, Poulas Konstantinos, Stavrou Eleana F, Papachatzopoulou Adamantia, Georgitsi Marianthi, Patrinos George |
Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA in ?-thalassaemia carriers. Archives of medical science : AMS 2021 8 17 (4): 1064-1074. Cyrus Cyril, Vatte Chittibabu, Chathoth Shahanas, Sayed Abdul Azeez, Borgio J Francis, Alrubaish Mohammed Abdullah, Alfalah Rawan, Alsaikhan Jana, Al Ali Amein |
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