(Q43057257)
Statements
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A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation (English)
1 reference
M S Enayat
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A M Guilliatt
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P E Short
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G Rastegar-Lari
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M Jazebi
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S Ravonbod
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F Ala
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O G Chapman
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F G H Hill
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1 November 2010
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16
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6
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966-969
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Identifiers
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1 reference