A case of incomplete achromatopsia of the deutan type

Author:

Van Norren D.,De Vries-De Mol E. C.

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Sensory Systems,Ophthalmology

Reference9 articles.

1. Hansen E (1979) Typical and atypical monochromacy studied by specific quantitative perimetry. Acta Ophthal 57:211?214

2. Pokorny J, Smith VC, Pinckers AJLG & Cozijnsen M (1981) Classification of complete and incomplete autosomal recessive achromatopsia. Graefes Arch Ophthal

3. Pokorny J, Smith VC & Swartley R (1979) Threshold measurements of spectral sensitivity in a blue monocone monochromat. Invest Ophthal 9: 807?813

4. Pokorny J, Smith VC, Verriest G & Pinckers AJLG (1979) Congenital and acquired color vision defects. Grune & Stratton, New York

5. Smith VC & Pokorny J (1980) Cone dysfunction syndromes defined by colour vision. In: Colour Vision Deficiencies V, ed. G. Verriest. Hilger, London

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The cone dysfunction syndromes;British Journal of Ophthalmology;2004-02-01

2. The cone dystrophies;Eye;1998-05

3. Classification of complete and incomplete autosomal recessive achromatopsia;Graefe's Archive for Clinical and Experimental Ophthalmology;1982-09

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