The DOI matches its Crossref record.
THE FAMILIAL DISTRIBUTION OF CONGENITAL TRITANOPIA: WITH SOME REMARKS ON SOME SIMILAR CONDITIONS
Abstract
Summary: Tritanopia was studied in forty‐seven affected individuals. Of these twenty‐two are propositi and twenty‐five relatives of propositi. The various tests used for the diagnosis of tritanopia are described and their efficiency is discussed. The familial incidence suggests that the bulk of congenital tritanopia is due to one or several autosomal dominant genes, with somewhat imperfect manifestation. On a single‐gene hypothesis, the incidence of the gene in England is estimated at about 1 in 20,000.
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“Inherited tritan color vision deficiencies are rare in comparison to the inherited red-green color vision defects and they have an autosomal dominant inheritance pattern (Kalmus, 1955).”
From The genetics of normal and defective color vision (2011) · cites this paper as Kalmus, 1955
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Research works printed but not linked: 24
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Cited by
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The Molecular Basis of Visual Excitation
WALD, G. (1968) · Nature · doi:10.1038/219800a0 · Cited by 824
The genetics of normal and defective color vision
Neitz, J., & Neitz, M. (2011) · Vision Research · doi:10.1016/j.visres.2010.12.002 · Cited by 377
MOLECULAR GENETICS OF HUMAN VISUAL PIGMENTS
Nathans, J., Merbs, S. L., Sung, C.-H., Weitz, C. J., & Wang, Y. (1992) · Annual Review of Genetics · doi:10.1146/annurev.ge.26.120192.002155 · Cited by 185
Metadata
- Authors
- KALMUS, H.
- Venue
- Annals of Human Genetics
- Publisher
- Wiley
- Published
- 1955-09
- Volume
- 20
- Issue
- 1
- Pages
- 39-56
- ISSN
- 0003-4800
- 1469-1809
- Cited by
- 48
- References
- 0
- Language
- en
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