DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
van Genderen MM, Bijveld MM, Claassen YB. et al.
Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.
Am J Hum Genet 2009;
85: 730-736
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