Olmsted syndrome with alopecia universalis caused by heterozygous mutation in PERP
- 30 July 2019
- journal article
- letter
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 182 (1) , 242-244
Abstract
No abstract availableKeywords
Funding Information
- National Natural Science Foundation of China (81573032, 81872515)
This publication has 8 references indexed in Scilit:
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- A NewTRPV3Missense Mutation in a Patient With Olmsted Syndrome and ErythromelalgiaJAMA Dermatology, 2014
- A Missense Mutation in the MBTPS2 Gene Underlies the X-Linked Form of Olmsted SyndromeJournal of Investigative Dermatology, 2013
- Exome Sequencing Reveals Mutations in TRPV3 as a Cause of Olmsted SyndromeThe American Journal of Human Genetics, 2012