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Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association DOCUMENTA OPHTHALMOLOGICA Marmor, M. F., Zeitz, C. 2018; 137 (1): 57–62
View details for DOI 10.1007/s10633-018-9651-0
View details for Web of Science ID 000440423900007