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Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram
Invest. Ophthalmol. Vis. Sci. Zeitz et al. 46: 4328

Supplementary Table

Christina Zeitz, Maria van Genderen, John Neidhardt, Ulrich F. O. Luhmann, Frank Hoeben, Ursula Forster, Katharina Wycisk, Gábor Mátyás, Carel B. Hoyng, Frans Riemslag, Françoise Meire, Frans P. M. Cremers, and Wolfgang Berger

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