Pages that link to "Q28144240"

The following pages link to Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa (Q28144240):

Displaying 14 items.

• RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa (Q24532214) (← links)
• Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains (Q28207567) (← links)
• Recent advances in the molecular basis of inherited photoreceptor degeneration (Q33942183) (← links)
• RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa (Q34559746) (← links)
• The complexities of ocular genetics (Q34592303) (← links)
• Mutations of RPGR in X-linked retinitis pigmentosa (RP3). (Q34610277) (← links)
• Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease (Q36467228) (← links)
• Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa (Q36683600) (← links)
• Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development (Q37471763) (← links)
• Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa (Q42631280) (← links)
• Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders (Q42684772) (← links)
• Analysis of RPGR in a South African family with X-linked retinitis pigmentosa: research and diagnostic implications. (Q46798132) (← links)
• Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications (Q48368986) (← links)
• Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype–phenotype correlations and impact on genetic counseling (Q56241301) (← links)