Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome.
Authors | 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 |
Journal | Human molecular genetics
(Hum Mol Genet)
Vol. 24
Issue 22
Pg. 6564
(Nov 15 2015)
ISSN: 1460-2083 [Electronic] England |
PMID | 26370416
(Publication Type: Published Erratum)
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