DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Audo I, Kohl S, Leroy BP. et al.
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Am J Hum Genet 2009;
85: 720-729
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