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Paper Details

An Unusual Retinal Phenotype Associated With a Mutation in Sterol Carrier Protein SCP2.
JAMA Ophthalmol
5
2017
Author NameAffiliation
Panagiotis I SergouniotisManchester Royal Eye Hospital, Central Manchester Foundation Trust, Saint Mary's Hospital
Rita HorvathJohn Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University
Graeme C M BlackManchester Royal Eye Hospital, Central Manchester Foundation Trust, Saint Mary's Hospital
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