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

Morarji, Jiten; Gillespie, Rachel; Sergouniotis, Panagiotis I; Horvath, Rita; Black, Graeme C M.

Afiliação

Morarji J; 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
Gillespie R; Manchester Centre for Genomic Medicine, Saint Mary's Hospital, Manchester Academic Health Science Centre, Central Manchester Foundation Trust, Manchester, United Kingdom.
Sergouniotis PI; 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
Horvath R; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle upon Tyne, United Kingdom.
Black GCM; 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

JAMA Ophthalmol ; 135(2): 167-169, 2017 Feb 01.

Article em En | MEDLINE | ID: mdl-28033445

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article