A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract (Q24655185)

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A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract
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    A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract (English)
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    A Arora
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    P J Minogue
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    X Liu
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    M A Reddy
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    J R Ainsworth
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    S S Bhattacharya
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    A R Webster
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    D M Hunt
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    L Ebihara
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    A T Moore
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    E C Beyer
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    V M Berthoud
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    January 2006
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    43
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    1
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    e2
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