Aims: To determine if asymptomatic carriers from a previously identified large pedigree of the Leber’s hereditary optic neuropathy (LHON) 11778 mtDNA mutation have colour vision deficits. Methods: As part of a compre...
Aims. This paper describes a novel test of colour vision using a standard pers onal computer, which is simple and reliable to perform. Methods. Twenty healthy individuals with normal colour vision and 10 healthy indiv...