Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia DefectsKonstantinos Nikopoulos, Carlo Rivolta, Nicola Bedoni et al.|The American Journal of Human Genetics|2016Cited by 60
Whole exome sequencing reveals CEP78 as a novel disease gene for cone-rod dystrophyKonstantinos Nikopoulos, Carlo Rivolta, Pietro Farinelli et al.|Investigative Ophthalmology & Visual Science|2016Cited by 1
Whole exome screening and identification of novel variants in a cohort of 28 Greek and Swedish families with cone-rod dystrophy.Nicola Bedoni, Carlo Rivolta, Konstantinos Nikopoulos et al.|Investigative Ophthalmology & Visual Science|2016Cited by 0