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Journal Abstract Search

166 related items for PubMed ID: 22190468

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  • 4. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.
    Tokgoz H, Torun Ozkan D, Caliskan U, Akar N.
    Platelets; 2015; 26(8):779-82. PubMed ID: 25734216
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  • 8. Linkage disequilibrium amongst ITGA2B and ITGB3 gene variants in patients with Glanzmann thrombasthenia confirms that most disease-causing mutations are recent.
    Pillois X, Nurden AT.
    Br J Haematol; 2016 Nov; 175(4):686-695. PubMed ID: 27469266
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  • 16. Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations.
    Zafarghandi Motlagh F, Fallah MS, Bagherian H, Shirzadeh T, Ghasri S, Dabbagh S, Jamali M, Salehi Z, Abiri M, Zeinali S.
    Orphanet J Rare Dis; 2019 Apr 27; 14(1):87. PubMed ID: 31029159
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  • 18. In silico analysis of structural modifications in and around the integrin αIIb genu caused by ITGA2B variants in human platelets with emphasis on Glanzmann thrombasthenia.
    Pillois X, Peters P, Segers K, Nurden AT.
    Mol Genet Genomic Med; 2018 Mar 27; 6(2):249-260. PubMed ID: 29385657
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  • 20. Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients.
    Fiore M, Firah N, Pillois X, Nurden P, Heilig R, Nurden AT.
    Haemophilia; 2012 May 27; 18(3):e201-9. PubMed ID: 22250950
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