Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypes (Q28274120)

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Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypes
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    Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypes (English)
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    T Kawano
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    Y Indo
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    H Nakazato
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    M Shimadzu
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    I Matsuda
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    5 June 1998
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    77
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    5
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    348-55
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