Updating and identifying a novel mutation in the PMVK gene in classic porokeratosis of Mibelli
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DOI: 10.1111/ced.13197
Abstract: Porokeratosis (OMIM 175800) is a heterogeneous group of keratinization disorders that exhibit an autosomal dominant mode of inheritance. Currently, there are around 20 clinical variants of PK in the English literature, which are classified by… read more here.
Keywords: gene; porokeratosis mibelli; porokeratosis; pmvk gene ... See more keywords