Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree

Background/aims: Familial exudative vitreoretinopathy (FEVR) is an inherited blinding condition characterised by abnormal development of the retinal vasculature. The aim of this study was to perform linkage analysis in a large family affected with FEVR to determine whether the mutation involved was...

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Detalhes bibliográficos
Main Authors: Toomes, C, Downey, L M, Bottomley, H M, Mintz-Hittner, H A, Inglehearn, C F
Formato: Artigo
Idioma:Inglês
Publicado em: Copyright 2005 British Journal of Ophthalmology 2005
Assuntos:
Clinical Science - Extended Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1772516/
https://ncbi.nlm.nih.gov/pubmed/15665352
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjo.2004.042507
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