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2066           Part XII:  Hemostasis and Thrombosis                                                                                                               Chapter 120:  Hereditary Qualitative Platelet Disorders        2067




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                 216. Nurden AT, Jallu V, Hourdille P: GP Ib and Bernard-Soulier platelets.  Blood 73:     245. Miller JL, Lyle VA, Cunningham D: Mutation of leucine-57 to phenylalanine in a plate-
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                  AD Michelson. Academic Press, San Diego, 2007.        246. Vettore S, Scandellari R, Moro S, et al: Novel point mutation in a leucine-rich repeat of
                 218. Lanza F, Baas MJ, Dupuis A, et al: Founder effect for a novel GPIBB mutations in Bernard-  the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, result-
                  Soulier patients from La Reunion island. J Thromb Haemost 11:1322 (abstract), 2013.  ing in an inherited dominant form of Bernard-Soulier syndrome affecting two unre-
                 219. Kenny D, Newman PJ, Morateck PA, Montgomery RR: A dinucleotide deletion results   lated families: The N41H variant. Haematologica 93:1743–1747, 2008.
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          Kaushansky_chapter 120_p2039-2072.indd   2066                                                                 9/21/15   2:22 PM
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