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Molecular genetic diagnosis of Tunisian Glanzmann thrombasthenia patients reveals a common nonsense mutation in the ITGA2B gene that seems to be specific for the studied population.
Aloui C, Chakroun T, Granados V, Jemni-Yacoub S, Fagan J, Khelif A, Kahloul N, Hammami S, Chkioua L, Barlier C, Cognasse F, Laradi S, Garraud O. Aloui C, et al. Among authors: granados v. Blood Coagul Fibrinolysis. 2018 Dec;29(8):689-696. doi: 10.1097/MBC.0000000000000779. Blood Coagul Fibrinolysis. 2018. PMID: 30325339
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