DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
den Hollander AI, Koenekoop RK, Yzer S. et al.
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.
Am J Hum Genet 2006;
79: 556-561
doi:10.1086/507318
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