Associated Papers
Expanding the spectrum of epidermodysplasia verruciformis: mutations linked to primary immunodeficiency disorders.
Sharma A et al.
Clinical and Experimental Dermatology, 2025
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.
Yuan B et al.
Genome Medicine, 2022
36180924 (PubMed )
Supplement: 13073_2022_1113_MOESM1_ESM.xlsx › Table_S6
Coronin-1A: immune deficiency in humans and mice.
Punwani D et al.
Journal of Clinical Immunology, 2015
Compound heterozygous CORO1A mutations in siblings with a mucocutaneous-immunodeficiency syndrome of epidermodysplasia verruciformis-HPV, molluscum contagiosum and granulomatous tuberculoid leprosy.
Stray-Pedersen A et al.
Journal of Clinical Immunology, 2014
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