Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome (Q55671532)

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Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome
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    Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome (English)
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    Huijun Wang
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    Xu Cao
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    Zhimiao Lin
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    Mingyang Lee
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    Xinying Jia
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    Yali Ren
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    Lanlan Dai
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    Liping Guan
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    Jianguo Zhang
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    Xuan Lin
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    Jie Zhang
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    Quan Chen
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    Cheng Feng
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    Eray Yihui Zhou
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    Jinghua Yin
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    Guiwen Xu
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    Yong Yang
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    1 January 2015
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    24
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    1
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    243-50
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