Case of Stargardt disease caused by uniparental isodisomy

Journal article

Open access

Peer reviewed

John H Fingert, David A Eliason, Nicole C Phillips, Andrew J Lotery, Val C Sheffield and Edwin M Stone

Archives of ophthalmology (1960), Vol.124(5), pp.744-745

05/2006

DOI: 10.1001/archopht.124.5.744

PMID: 16682602

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url

https://doi.org/10.1001/archopht.124.5.744View

Published (Version of record) Open Access

no abstract

Polymerase Chain Reaction

Genetic Markers

Mutation

ATP-Binding Cassette Transporters - genetics

Macular Degeneration - genetics

Pedigree

Humans

Adolescent

Uniparental Disomy

Female

Genotype

Visual Acuity

Title: Subtitle: Case of Stargardt disease caused by uniparental isodisomy
Creators: John H Fingert - Dept. of Ophthalmology, University of Iowa College of Medicine, Iowa City, IA 52242, USA. edwin-stone@uiowa.edu
David A Eliason
Nicole C Phillips
Andrew J Lotery
Val C Sheffield
Edwin M Stone
Resource Type: Journal article
Publication Details: Archives of ophthalmology (1960), Vol.124(5), pp.744-745
DOI: 10.1001/archopht.124.5.744
PMID: 16682602
NLM abbreviation: Arch Ophthalmol
ISSN: 0003-9950
eISSN: 1538-3601
Publisher: American Medical Association; United States
Language: English
Date published: 05/2006
Academic Unit: Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Medical Genetics and Genomics; Ophthalmology and Visual Sciences
Record Identifier: 9983979972502771

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