Complete exon-intron structure of the retina-specific ATP binding transporter gene (ABCR) allows the identification of novel mutations underlying Stargardt disease (Q28264805)

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Complete exon-intron structure of the retina-specific ATP binding transporter gene (ABCR) allows the identification of novel mutations underlying Stargardt disease
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    Complete exon-intron structure of the retina-specific ATP binding transporter gene (ABCR) allows the identification of novel mutations underlying Stargardt disease (English)
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    S Gerber
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    T J van de Pol
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    C B Hoyng
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    A Blankenagel
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    J Kaplan
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    F P Cremers
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    15 February 1998
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    48
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    1
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    139-42
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