Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families (Q24678278)
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Current Data About Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families
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(P1476) "Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families" (language: en)
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(P2093) M Buraczynska
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L Gieser
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W Wu
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P Forsythe
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M Abrahamson
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S G Jacobson
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S Andréasson
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A Swaroop
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