Eksandh L, Kohl S, Wissinger B (June 2002). "Clinical features of achromatopsia in Swedish patients with defined genotypes". Ophthalmic Genet. 23 (2): 109–20. doi:10.1076/opge.23.2.109.2210. PMID12187429. S2CID25718360.
Eksandh L, Kohl S, Wissinger B (June 2002). "Clinical features of achromatopsia in Swedish patients with defined genotypes". Ophthalmic Genet. 23 (2): 109–20. doi:10.1076/opge.23.2.109.2210. PMID12187429. S2CID25718360.
Eksandh L, Kohl S, Wissinger B (June 2002). "Clinical features of achromatopsia in Swedish patients with defined genotypes". Ophthalmic Genet. 23 (2): 109–20. doi:10.1076/opge.23.2.109.2210. PMID12187429. S2CID25718360.
Weleber RG (June 2002). "Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)". Ophthalmic Genet. 23 (2): 71–97. doi:10.1076/opge.23.2.71.2214. PMID12187427. S2CID30741530.