Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies.
[This corrects the article DOI: 10.1371/journal.pone.0169226.].
Main Authors: | Hyun-Seok Jin, Jeonghyung Kim, Woori Kwak, Hyeonsoo Jeong, Gyu-Bin Lim, Cha Gon Lee |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2017-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC5340411?pdf=render |
Similar Items
-
Novel MIP gene mutation causes autosomal-dominant congenital cataract
by: Jing-Lan Ni, et al.
Published: (2024-03-01) -
A Novel Mutation in CRYGC Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea
by: Zhenbao Zhou, MD, et al.
Published: (2022-03-01) -
Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract
by: Li Wang, et al.
Published: (2016-01-01) -
A Novel CRYBB2 Stopgain Mutation Causing Congenital Autosomal Dominant Cataract in a Chinese Family
by: Yu Zhou, et al.
Published: (2016-01-01) -
A novel GJA8 mutation (p.V44A) causing autosomal dominant congenital cataract.
by: Yanan Zhu, et al.
Published: (2014-01-01)