Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis. (Q34088707)
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Current Data About Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis.
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(P1476) "Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis" (language: en)
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(P2093) Hanein S
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Barbet F
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Ducroq D
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Ghazi I
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Martin-Coignard D
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Leowski C
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Homfray T
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Dufier JL
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Kaplan J
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Munnich A
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