An Unusual Retinal Phenotype Associated With a Mutation in Sterol Carrier Protein SCP2

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Journal

Title: JAMA Ophthalmology

Abbreviated Title: JAMA Ophthalmol

Publisher: American Medical Association (AMA)

ISSN (Print): 2168-6165

Publication date Created: February 01 2017

Publication date (Print): February 01 2017

Volume: 135

Issue: 2

Page: 167

Affiliations

[1 ]Manchester Royal Eye Hospital, Manchester Academic Health Science Centre, Central Manchester Foundation Trust, Manchester, United Kingdom2Manchester Centre for Genomic Medicine, Saint Mary’s Hospital, Manchester Academic Health Science Centre, Central Manchester Foundation Trust, Manchester, United Kingdom

[2 ]Manchester Centre for Genomic Medicine, Saint Mary’s Hospital, Manchester Academic Health Science Centre, Central Manchester Foundation Trust, Manchester, United Kingdom

[3 ]John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle upon Tyne, United Kingdom

Article

DOI: 10.1001/jamaophthalmol.2016.4985

PubMed ID: 28033445

SO-VID: ff13276f-e944-46b9-9922-e5358f82e66a

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