Identifying variation in models of care for the genomic-based diagnosis of inherited retinal dystrophies in the United Kingdom

PURPOSE: Advances in genomic technologies are prompting a realignment of diagnostic and management pathways for rare inherited disease. New models of care are being developed as genomic-based diagnostic testing becomes increasingly relevant within more and more aspects of medicine. This study descri...

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Bibliographic Details
Published in:Eye (Lond)
Main Authors: Eden, M, Payne, K, Jones, C, Wright, S J, Hall, G, McAllister, M, Black, G
Format: Artigo
Language:Inglês
Published: Nature Publishing Group 2016
Subjects:
Clinical Study
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4941073/
https://ncbi.nlm.nih.gov/pubmed/27080487
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/eye.2016.74
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