Functional consequences of pathogenic variant c.61G>C in the inflammasome gene NLRP3 underlying keratitis fugax hereditaria.
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| Title: | Functional consequences of pathogenic variant c.61G>C in the inflammasome gene NLRP3 underlying keratitis fugax hereditaria. |
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| Authors: | Kawan S; Eye Genetics Group, Folkhälsan Research Center, Helsinki, Finland.; Department of Ophthalmology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland., Backlund MP; Eye Genetics Group, Folkhälsan Research Center, Helsinki, Finland., Immonen AT; Eye Genetics Group, Folkhälsan Research Center, Helsinki, Finland.; Department of Ophthalmology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland., Kivelä TT; Department of Ophthalmology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland., Turunen JA; Eye Genetics Group, Folkhälsan Research Center, Helsinki, Finland joni.turunen@helsinki.fi.; Department of Ophthalmology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. |
| Source: | The British journal of ophthalmology [Br J Ophthalmol] 2024 Jan 29; Vol. 108 (2), pp. 323-328. Date of Electronic Publication: 2024 Jan 29. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 0421041 Publication Model: Electronic Cited Medium: Internet ISSN: 1468-2079 (Electronic) Linking ISSN: 00071161 NLM ISO Abbreviation: Br J Ophthalmol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1468-2079 |
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| DOI: | 10.1136/bjo-2022-321825 |
