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Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361588/
https://www.ncbi.nlm.nih.gov/pubmed/25775450
http://dx.doi.org/10.1371/journal.pone.0120166
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spelling pubmed-43615882015-03-23 Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies PLoS One Correction Public Library of Science 2015-03-16 /pmc/articles/PMC4361588/ /pubmed/25775450 http://dx.doi.org/10.1371/journal.pone.0120166 Text en © 2015 The PLOS ONE Staff http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Correction
Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
title Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
title_full Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
title_fullStr Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
title_full_unstemmed Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
title_short Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
title_sort correction: exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361588/
https://www.ncbi.nlm.nih.gov/pubmed/25775450
http://dx.doi.org/10.1371/journal.pone.0120166
work_keys_str_mv AT correctionexomesequencingrevealsnovelandrecurrentmutationswithclinicalsignificanceininheritedretinaldystrophies