Hereditary Choroidal Dystrophy
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-16-7337-5_16
Reference23 articles.
1. Rafuse EV, McCulloch C. Choroideremia. A pathological report. Can J Ophthalmol. 1968;3:347–52.
2. Rubin ML, Fishman RS, McKay RA. Choroideremia. Study of a family and literature review. Arch Ophthalmol. 1966;76:563–74.
3. van den Hurk JA, Schwartz M, van Bokhoven H, van de Pol TJ, Bogerd L, Pinckers AJ, et al. Molecular basis of choroideremia (CHM): mutations involving the Rab escort protein-1 (REP-1) gene. Hum Mutat. 1997;9:110–7.
4. Pennesi ME, Birch DG, Duncan JL, Bennett J, Girach A. CHOROIDEREMIA: retinal degeneration with an unmet need. Retina. 2019;39:2059–69.
5. Jolly JK, Xue K, Edwards TL, et al. Characterizing the natural history of visual function in choroideremia using microperimetry and multimodal retinal imaging. Invest Ophthalmol Vis Sci. 2017;58:5575–83.
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