Exome sequencing in a Chinese family reveals TTC9 mutation associated with keratitis-ichthyosis-deafness (KID) syndrome.
| Autor: | Xiaohua WANG, Xueli WU, Baoqing ZHENG, Yongfeng CHEN, Daocheng ZHENG |
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| Zdroj: | European Journal of Dermatology; Jul/Aug2018, Vol. 28 Issue 4, p534-535, 2p |
| Databáze: | Complementary Index |
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