Stufendiagnostik einer CSNB1 mit NYX-Genmutation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s00347-019-0886-2.pdf
Reference9 articles.
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2. Heon E, Musarella MA (1994) Congenital stationary night blindness: A critical review for molecular approaches. In: Wright AF, Jay B (Hrsg) Molecular genetics of inherited eye disorders. Harwood Academic, Chur, S 277–301
3. Kurata K, Hosono K, Hotta Y (2017) Long-term clinical course in a patient with complete congenital stationary night blindness. Case Rep Ophthalmol 8(1):237–244
4. Lagreze WA, Schaeffel F (2017) Preventing myopia. Dtsch Arztebl Int 114(35/36):575–580
5. Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T (1986) Congenital stationary night blindness with negative electroretinogram: A new classification. Arch Ophthal 104:1013–1020
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