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Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies

Detalles Bibliográficos
Autores principales: Jin, Hyun-Seok, Kim, Jeonghyung, Kwak, Woori, Jeong, Hyeonsoo, Lim, Gyu-Bin, Lee, Cha Gon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340411/
https://www.ncbi.nlm.nih.gov/pubmed/28267770
http://dx.doi.org/10.1371/journal.pone.0173757
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author Jin, Hyun-Seok
Kim, Jeonghyung
Kwak, Woori
Jeong, Hyeonsoo
Lim, Gyu-Bin
Lee, Cha Gon
author_facet Jin, Hyun-Seok
Kim, Jeonghyung
Kwak, Woori
Jeong, Hyeonsoo
Lim, Gyu-Bin
Lee, Cha Gon
author_sort Jin, Hyun-Seok
collection PubMed
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spelling pubmed-53404112017-03-29 Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies Jin, Hyun-Seok Kim, Jeonghyung Kwak, Woori Jeong, Hyeonsoo Lim, Gyu-Bin Lee, Cha Gon PLoS One Correction Public Library of Science 2017-03-07 /pmc/articles/PMC5340411/ /pubmed/28267770 http://dx.doi.org/10.1371/journal.pone.0173757 Text en © 2017 Jin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Correction
Jin, Hyun-Seok
Kim, Jeonghyung
Kwak, Woori
Jeong, Hyeonsoo
Lim, Gyu-Bin
Lee, Cha Gon
Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies
title Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies
title_full Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies
title_fullStr Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies
title_full_unstemmed Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies
title_short Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies
title_sort correction: identification of a novel mutation in brd4 that causes autosomal dominant syndromic congenital cataracts associated with other neuro-skeletal anomalies
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340411/
https://www.ncbi.nlm.nih.gov/pubmed/28267770
http://dx.doi.org/10.1371/journal.pone.0173757
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