Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome

Human Molecular Genetics, 2015, Vol. 24, No. 22 6564 doi: 10.1093/hmg/ddv365 Advance Access Publication Date: 14 September 2015 Corrigendum CORRIGENDUM Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosisleukonychia totalis syndrome Huijun Wang, Xu Cao, Zhimiao Lin, Mingyang Lee, Xinying Jia, Yali Ren, Lanlan Dai, Liping Guan, Jianguo Zhang, Xuan Lin, Jie Zhang, Quan Chen, Cheng Feng, Eray Yihui Zhou, Jinghua Yin, Guiwen Xu and Yong Yang Human Molecular Genetics 2015 24:1; pp. 243–250; doi: 10.1093/hmg/ ddu442 The authors apologize for the errors made in the second part of the Result section. In all cases, the mutation should be c.23G>T rather than c.23G>A. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: 6564  (...truncated)