Ann Dermatol.
2021 Apr;33(2):198-200. 10.5021/ad.2021.33.2.198.
A Case of Familial Cold Autoinflammatory Syndrome with De Novo NLRP3 Mutation
- Affiliations
-
- 1Department of Dermatology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, China
- 2Institute of Dermatology, Shanghai Jiao Tong University School of Medicine, Shanghai, China
- KMID: 2513606
- DOI: http://doi.org/10.5021/ad.2021.33.2.198
- Full Text Links
-
- Actions
-
Cited
- CITED
-
- Close
- Share
-
- Similar articles
-
- Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A
- De novo Formation of Familial Cerebral Aneurysms
- The First Case Series of Cryopyrin-Associated Periodic Syndrome in Korea
- Identification of a Novel De Novo Mutation of the TAZ Gene in a Korean Patient with Barth Syndrome
- The First Case of a Korean Patient with a MutationConfirmed Tumor Necrosis Factor Receptor-Associated Periodic Syndrome
