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

AuthorsHuijun 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
JournalHuman molecular genetics (Hum Mol Genet) Vol. 24 Issue 22 Pg. 6564 (Nov 15 2015) ISSN: 1460-2083 [Electronic] England
PMID26370416 (Publication Type: Published Erratum)

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