Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR (Q28262021)

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Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR
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    Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR (English)
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    F P Cremers
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    D J van de Pol
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    M van Driel
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    A I den Hollander
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    F J van Haren
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    N V Knoers
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    N Tijmes
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    A A Bergen
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    K Rohrschneider
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    A Blankenagel
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    A J Pinckers
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    A F Deutman
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    C B Hoyng
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    March 1998
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    7
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    355-62
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    3
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