Exome sequencing in a Chinese family reveals TTC9 mutation associated with keratitis-ichthyosis-deafness (KID) syndrome
| Autor: | Baoqing Zheng, Xiaohua Wang, Xueli Wu, Yongfeng Chen, Daocheng Zheng |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Genetics
Adult Keratitis Male China business.industry Nerve Tissue Proteins Dermatology Pedigree 030207 dermatology & venereal diseases 03 medical and health sciences Keratitis ichthyosis deafness 0302 clinical medicine 030220 oncology & carcinogenesis Mutation (genetic algorithm) Mutation Exome Sequencing Medicine Humans Female Chinese family business Child Exome sequencing Kid syndrome |
| Zdroj: | European journal of dermatology : EJD. 28(4) |
| ISSN: | 1952-4013 |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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