Similar Items: Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort
- Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study
- Spinocerebellar ataxias
- At-risk individual's perspectives of Spinocerebellar Ataxia (SCA) Presymptomatic Testing (PT)
- An intronic variant in Ferredoxin Reductase (FDXR) creates a cryptic exon in Quarter Horses with Equine Juvenile Spinocerebellar Ataxia
- Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene
- The pathogenesis of HIV-associated cardiomyopathy : a histological, virological, and genetic study
Author: Greenberg, Jacquie
- An investigation into the level of genetic knowledge of parents of sons with Duchenne Muscular Dystrophy and their satisfaction with the genetic counselling service at Red Cross War Memorial Children's Hospital
- A molecular investigation of the novel gene underlying autosomal dominant retinitis pigmentosa in a South African family
- Mutation analysis of important retinal candidate genes: progression from research to diagnostic service
- Hereditary nonpolyposis colorectal cancer : factors contributing to adherence and non-adherence to surveillance for mutation carriers in rural areas of the Northern and Western Cape Brenda Julie Kruger.
- Detailed investigation of the unstable (CAG) repeat and the immediate surrounding region of the IT15 gene in some South African families with Huntington disease
- RNAi based allele-specific silencing of the disease-causing gene in black South African patients with SCA7