DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Zeitz C, van Genderen M, Neidhardt J. et al.
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
Invest Ophthalmol Vis Sci 2005;
46: 4328-4335
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