Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene (Q28256664)

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Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene
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    Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene (English)
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    Yuko Wada
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    Toshitaka Itabashi
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    Hajime Sato
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    Makoto Tamai
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    November 2004
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    242
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    11
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    956-61
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