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Paper Details

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Hum Mutat
9
2022
Author NameAffiliation
David G BirchRetina Foundation of the Southwest
H??l??ne DollfusHopitaux Universitaires de Strasbourg
H??l??ne DollfusInserm, Universite de Strasbourg
Samuel G JacobsonPerelman School of Medicine, Scheie Eye Institute, University of Pennsylvania
Franco StanzialClinical Genetics Service and South Tyrol Coordination Center for Rare Diseases, Regional Hospital of Bolzano
Richard G WeleberOregon Health & Science University, Ophthalmic Genetics Service of the Casey Eye Institute
Katarina StinglCenter for Ophthalmology, University Eye Hospital, University of Tubingen
Katarina StinglCenter for Rare Eye Diseases, University of Tubingen
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