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Fujita et al., 1997 - Google Patents

Analysis of the RPGRGene in 11 Pedigrees with the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two …

Fujita et al., 1997

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Document ID
14850174054075246365
Author
Fujita R
Buraczynska M
Gieser L
Wu W
Forsythe P
Abrahamson M
Jacobson S
Sieving P
Andréasson S
Swaroop A
Publication year
Publication venue
The American Journal of Human Genetics

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X-linked retinitis pigmentosa (XLRP) is a severe form of inherited progressive retinal degeneration. The RP3 (retinitis pigmentosa type 3) locus at Xp21. 1 is believed to account for the disease in the majority of XLRP families. Linkage analysis and identification of …
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