DL Thiselton

OPA1, encoding a dynamin-related GTPase is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

C B Alexander, Marcela Votruba, U. E.A. Pesch et al. · American Journal of Ophthalmology · 2001 · 41 citations

Mutations in the RP2 gene cause disease in 10% of familial XLRP assessed in this study

DL Thiselton, Lionel Van Maldergem, B K Saha et al. · UCL Discovery (University College London) · 1999 · 10 citations