Associated Papers
A novel homozygous variant in PMVK is associated with enhanced IL1β secretion and a hyper-IgD syndrome-like phenotype.
Jairaman A et al.
Clinical Genetics, 2024
A Novel PMVK Variant Associated with Familial Porokeratosis.
Zhang W et al.
Human Heredity, 2023
Updating and identifying a novel mutation in the PMVK gene in classic porokeratosis of Mibelli.
Song NJ et al.
Clinical and Experimental Dermatology, 2017
Mutation Analysis of the MVD Gene in a Chinese Family with Disseminated Superficial Actinic Porokeratosis and a Chinese Literature Review.
Qian W et al.
Indian Journal of Dermatology, 0
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