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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.
Authors:R Fujita, M Buraczynska, L Gieser, W Wu, P Forsythe, M Abrahamson, S G Jacobson, P A Sieving, S Andr  asson,   A Swaroop
Affiliation:R Fujita, M Buraczynska, L Gieser, W Wu, P Forsythe, M Abrahamson, S G Jacobson, P A Sieving, S Andréasson, and A Swaroop
Abstract:
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