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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, Yong Yang, Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome, Human Molecular Genetics, Volume 24, Issue 22, 15 November 2015, Page 6564, https://doi.org/10.1093/hmg/ddv365
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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: [email protected]
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