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ARVO Annual Meeting Abstract July 2018

Homozygous mutations in KIAA1549 , encoding a ciliary protein, cause autosomal recessive retinitis pigmentosa.

Susanne Roosing; Suzanne E. de Bruijn; Sanne Kirsten Verbakel; Hannie Kremer; L. Ingeborgh van den Born; Carel C B Hoyng; Frans P Cremers

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2321. doi:

ARVO Annual Meeting Abstract June 2017

Insensitive short-term clinical trial endpoint in Stargardt disease: progression of best-corrected visual acuity

Sanne Kirsten Verbakel; Stanley Lambertus; Nathalie Bax; Dyon Valkenburg; Ramon van Huet; Joannes Groenewoud; Carel C B Hoyng

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2014. doi:

ARVO Annual Meeting Abstract September 2016

Acetazolamide for the treatment of cystic macular lesions in children and young adults with hereditary macular dystrophies

Sanne Kirsten Verbakel; John van de Ven; Linda M.P. Le Blanc; Joannes M.M. Groenewoud; Eiko de Jong; Carel C B Hoyng

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2699. doi:

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