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Paper Details

A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430Aâ¿¿>â¿¿G in retinoid isomerohydrolase (RPE65) and c.37Câ¿¿>â¿¿T in bestrophin 1 (BEST1).
Doc Ophthalmol
1
2021
Author NameAffiliation
Fred K ChenCentre for Ophthalmology and Visual Science (Incorporating Lions Eye Institute), The University of Western Australia
Fred K ChenSir Charles Gairdner Hospital
Fred K ChenRoyal Perth Hospital
Fred K ChenPerth Children's Hospital
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Release 1.2