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Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram
Zeitz, Christina, van Genderen, Maria, Neidhardt, John, Luhmann, Ulrich F. O., Hoeben, Frank, Forster, Ursula, Wycisk, Katharina, Ma´tya´s, Ga´bor, Hoyng, Carel B., Riemslag, Frans, Meire, Franc¸oise,Volume:
46
Language:
english
Journal:
Investigative Opthalmology & Visual Science
DOI:
10.1167/iovs.05-0526
Date:
November, 2005
File:
PDF, 476 KB
english, 2005