genetics

Determining the functional disparty between CRB1 variants causing LCA and RP
Leveraging cutting-edge model systems to further understand CRB1-related eye disease
Nicholas Owen
Determining the functional disparty between CRB1 variants causing LCA and RP
Rare disease genetic diagnosis with the Genomic England 100,000 Genomes Project (GEL) UK
collaborative research with the Hearing and Sight GECIP at GEL
Nicholas Owen
Rare disease genetic diagnosis with the Genomic England 100,000 Genomes Project (GEL) UK