Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA (Q24310410)

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Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
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    Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA (English)
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    M Litt
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    P Kramer
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    D M LaMorticella
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    W Murphey
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    E W Lovrien
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    R G Weleber
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    March 1998
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    7
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    3
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    471-4
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