Pages that link to "Q36903002"

The following pages link to Analysis of a large choroideremia dataset does not suggest a preference for inclusion of certain genotypes in future trials of gene therapy (Q36903002):

Displaying 14 items.

• The Spectrum of CHM Gene Mutations in Choroideremia and Their Relationship to Clinical Phenotype. (Q37404457) (← links)
• Unravelling the genetic basis of simplex Retinitis Pigmentosa cases (Q37623694) (← links)
• Hereditary Retinal Dystrophy (Q39051446) (← links)
• Novel non-contiguous exon duplication in choroideremia. (Q45866412) (← links)
• Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapy (Q45871948) (← links)
• Single-base substitutions in the CHM promoter as a cause of choroideremia. (Q50856170) (← links)
• A Qualitative and Quantitative Assessment of Fundus Autofluorescence Patterns in Patients With Choroideremia. (Q51768847) (← links)
• The effect of PTC124 on choroideremia fibroblasts and iPSC-derived RPE raises considerations for therapy. (Q55025407) (← links)
• Novel CHM mutations in Polish patients with choroideremia - an orphan disease with close perspective of treatment (Q60045520) (← links)
• Nonsense-mediated mRNA decay efficiency varies in choroideremia providing a target to boost small molecule therapeutics (Q64261224) (← links)
• Synonymous Variant in the CHM Gene Causes Aberrant Splicing in Choroideremia (Q89876476) (← links)
• Molecular Therapies for Choroideremia (Q90241422) (← links)
• Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families (Q100307115) (← links)
• Expanding the genetic spectrum of choroideremia in an Australian cohort: report of five novel CHM variants (Q101039835) (← links)