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    Journal Articles

    A mutation in the Gardos channel is associated with hereditary xerocytosis

    Raphael Rapetti-Mauss, Caroline Lacoste, Véronique Picard, Corinne Guitton, Elise Lombard, Marie Loosveld, Vanessa Nivaggioni, Nathalie Dasilva, David Salgado, Jean-Pierre Desvignes, Christophe Béroud, Patrick Viout, Monique Bernard, Olivier Soriani, Henri Vinti, Valérie Lacroze, Madeleine Feneant-Thibault, Isabelle Thuret, Hélène Guizouarn, Catherine Badens
    Journal: Blood
    Blood (2015) 126 (11): 1273–1280.
    https://doi.org/10.1182/blood-2015-04-642496
    Published: 2015
    Journal Articles

    Fibrinogen Alès: a homozygous case of dysfibrinogenemia (γ-Asp 330 →Val) characterized by a defective fibrin polymerization site “a”

    Karim Chabane Lounes, Claudine Soria, Shah Sultan Mirshahi, Pierre Desvignes, Massoud Mirshahi, Olivier Bertrand, Pierre Bonnet, Jaap Koopman, Jeannette Soria
    Journal: Blood
    Blood (2000) 96 (10): 3473–3479.
    https://doi.org/10.1182/blood.V96.10.3473
    Published: 2000

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