Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis (Q24313340)

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Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis
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    Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis (English)
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    S W Eber
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    J M Gonzalez
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    M L Lux
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    A L Scarpa
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    W T Tse
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    M Dornwell
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    J Herbers
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    W Kugler
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    R Ozcan
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    A Pekrun
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    P G Gallagher
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    W Schröter
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    B G Forget
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    S E Lux
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    June 1996
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    13
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    214-8
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    2
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