Associated Papers
Loricrin keratoderma: description of a novel mutation, systematic review and meta-analysis between genotypic and phenotypic features.
Montero-Vilchez T et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : Jddg, 2020
A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma.
Kinsler VA et al.
The British Journal of Dermatology, 2015
Select a paper to view details