DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Vincent A, Audo I, Tavares E. et al.
Biallelic mutations in GNB3 cause a unique form of autosomal-recessive congenital stationary night blindness.
Am J Hum Genet 2016;
98: 1011-1019
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