Associated Papers
Epidermal second-hit mutation in MVK gene associated with linear porokeratosis.
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Genes & Diseases, 2025
39386107 (PubMed )
Supplement: mmc2.xlsx › standard
Genetic Risk Factors for Nontuberculous Mycobacterial Pulmonary Disease (Systematic Review).
Sviridov PS et al.
Sovremennye Tekhnologii V Meditsine, 2024
Genetic Landscape of Rare Autoinflammatory Disease Variants in Qatar and Middle Eastern Populations Through the Integration of Whole-Genome and Exome Datasets.
Sharma P et al.
Frontiers in Genetics, 2021
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Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P.
Hoffman HM et al.
Human Genetics, 2003
Analysis of NLRP3, MVK and TNFRSF1A variants in adult Greek patients with autoinflammatory symptoms.
Karagianni P et al.
Clinical and Experimental Rheumatology, 0
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