학술논문
Corrigendum: Opportunities and Challenges for Molecular Understanding of Ciliopathies–The 100,000 Genomes Project.
Document Type
Correction Notice
Author
Wheway, Gabrielle; Mitchison, Hannah M.; Ambrose, J. C.; Baple, E. L.; Bleda, M.; Boardman-Pretty, F.; Boissiere, J. M.; Boustred, C. R.; Caulfield, M. J.; Chan, G. C.; Craig, C. E. H.; Daugherty, L. C.; de, Burca A.; Devereau, A.; Elgar, G.; Foulger, R. E.; Fowler, T.; Furió-Tarí, P.; Hackett, J. M.; Halai, D.
Source
Frontiers in Genetics; 8/13/2019, p1-2, 2p
Subject
Language
ISSN
16648021
Abstract
Highlights from the article: Suitable gene panels with features overlapping the phenotype e.g., retinal dystrophy gene panel, Protein altering variants affecting genes not in the virtual gene 100,000 Genomes Project uses data provided by patients and Copyright of Frontiers in Genetics is the property of Frontiers Media S.A. and its content may.