DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Audo I, Bujakowska K, Orhan E. et al.
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Am J Hum Genet 2012;
90: 321-330
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