Cargando…
Correction: Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies
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 |
_version_ | 1782361663167528960 |
---|---|
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-4361588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |