Carolyn I. Hope
Department of Ophthalmology
University of Auckland
Auckland
New Zealand
Name/email consistency: high
- Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2. Hope, C.I., Sharp, D.M., Hemara-Wahanui, A., Sissingh, J.I., Lundon, P., Mitchell, E.A., Maw, M.A., Clover, G.M. Clin. Experiment. Ophthalmol. (2005)