Pages that link to "Q40477868"
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The following pages link to Clinical findings in a carrier of a new mutation in the choroideremia gene. (Q40477868):
Displaying 14 items.
- Silencing of the CHM gene alters phagocytic and secretory pathways in the retinal pigment epithelium (Q33845316) (← links)
- Choroideremia associated with choroidal neovascularization treated with intravitreal bevacizumab (Q34156471) (← links)
- Cystic macular oedema on spectral-domain optical coherence tomography in choroideremia patients without cystic changes on fundus examination (Q34490245) (← links)
- Clinical characteristics and current therapies for inherited retinal degenerations (Q35045067) (← links)
- Pathogenic mechanisms and the prospect of gene therapy for choroideremia. (Q35910610) (← links)
- Transition Zones between Healthy and Diseased Retina in Choroideremia (CHM) and Stargardt Disease (STGD) as Compared to Retinitis Pigmentosa (RP) (Q35925184) (← links)
- Choroideremia: analysis of the retina from a female symptomatic carrier (Q36838709) (← links)
- Analysis of a large choroideremia dataset does not suggest a preference for inclusion of certain genotypes in future trials of gene therapy (Q36903002) (← links)
- Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia (Q37661650) (← links)
- Clinical characteristics of a large choroideremia pedigree carrying a novel CHM mutation (Q37700064) (← links)
- A novel mutation (967-970 2)delAAAGGT in the choroideremia gene found in a Japanese family and related clinical findings (Q38287737) (← links)
- Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers (Q47684282) (← links)
- Choroideremia: Effect of age on visual acuity in patients and female carriers (Q50995412) (← links)
- Expanding the genetic spectrum of choroideremia in an Australian cohort: report of five novel CHM variants (Q101039835) (← links)