Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis (Q24642869)

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Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis
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    Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis (English)
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    Sara J Bowne
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    Lori S Sullivan
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    Sarah E Mortimer
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    Lizbeth Hedstrom
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    Jingya Zhu
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    Catherine J Spellicy
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    Anisa I Gire
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    Dianna Hughbanks-Wheaton
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    Richard A Lewis
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    John R Heckenlively
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    January 2006
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    47
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    1
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    34-42
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