Mutations in CERS3 Gene Underlies a Case of Autosomal Recessive Congenital Ichthyosis

Autosomal recessive congenital ichthyosis caused by CERS3 mutations is extremely rare in clinical practice. We recently identified a family of autosomal recessive congenital ichthyosis and performed multigene exome sequencing for hereditary skin diseases to identify causative genes. Mutation analysi...

書目詳細資料
發表在:	罕见病研究
Main Authors:	LIU Juan, MO Ran, LIU Yihe, HUANG Xin, GAO Meng, YANG Yong, CHEN Zhiming
格式:	Article
語言:	中文
出版:	Editorial Office of Journal of Rare Diseases 2023-04-01
主題:	autosomal recessive congenital ichthyosis cers3 gene exon deletion acitretin
在線閱讀:	https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2023.02.016

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