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References
Wright WD (1952) The characteristics of the tritanopia. J Opt Soc Am 42:509–521
Terasaki H, Miyake Y, Awaya S, Horio N (1995) Visual functions of dominantly inherited juvenile optic atrophy. Acta Soc Ophthalmol Jpn 99:964–971
Krill AE, Smith VC, Pokorny J (1970) Similarities between congenital tritan defects and dominant opticus-atrophy: coincidence or identity? J Opt Soc Am 60:1132–1139
Krill AE, Smith VG, Pokorny J (1971) Further studies supporting identity of congenital tritanopia and hereditary dominant optic atrophy. Invest Ophthalmol 15:457–465
Miyake Y, Yagasaki K, Ichikawa H (1985) Differential diagnosis of congenital tritanopia and dominantly inherited juvenile optic atrophy. Arch Ophthalmol 103:1496–1501
Weitz CJ, Miyake Y, Shinzato K, Montag E, Zrenner E, Went LN, Nathans J (1992) Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin. Am J Hum Genet 50:498–507
Votruba M, Moore AT, Bhattacharya SS, et al. (1997) Genetic refinement of dominant optic atrophy (OPA1) locus to within in a 2 CM interval of chromosome 3q. J Med Genet 34:117–121
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(2006). Congenital Tritanopia—Differential Diagnosis of Dominantly Inherited Juvenile Optic Atrophy. In: Electrodiagnosis of Retinal Diseases. Springer, Tokyo. https://doi.org/10.1007/4-431-30306-5_21
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DOI: https://doi.org/10.1007/4-431-30306-5_21
Publisher Name: Springer, Tokyo
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