Ontology highlight
ABSTRACT:
SUBMITTER: Doron R
PROVIDER: S-EPMC6343896 | biostudies-literature | 2019
REPOSITORIES: biostudies-literature
Doron Ravid R Sterkin Anna A Fried Moshe M Yehezkel Oren O Lev Maria M Belkin Michael M Rosner Mordechai M Solomon Arieh S AS Mandel Yossi Y Polat Uri U
PloS one 20190123 1
Color deficiency is a common inherited disorder affecting 8% of Caucasian males with anomalous trichromacy (AT); it is the most common type of inherited color vision deficiency. Anomalous trichromacy is caused by alteration of one of the three cone-opsins' spectral sensitivity; it is usually considered to impose marked limitations for daily life as well as for choice of occupation. Nevertheless, we show here that anomalous trichromat subjects have superior basic visual functions such as visual a ...[more]