A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case report.
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| Title: | A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case report. |
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| Authors: | Li, Yue1,2 (AUTHOR), Wang, Yumeng1 (AUTHOR), Ming, Yan1 (AUTHOR), Chaolan, Pan1 (AUTHOR), Jia, Zhang1 (AUTHOR), Cheng, Ni1 (AUTHOR), Qiaoyu, Cao1 (AUTHOR), Li, Ming1,3 (AUTHOR) liming01@xinhuamed.com.cn, Tianyi, Xu4 (AUTHOR) lmxuty@163.com |
| Source: | BMC Medical Genomics. 11/1/2021, Vol. 14 Issue 1, p1-7. 7p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 17558794 |
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| DOI: | 10.1186/s12920-021-01109-4 |
