Associated Papers
A rare case of LORICRIN gene c.684dup mutation associated with Vohwinkel syndrome in a Turkish patient, in silico analysis and literature review.
Yavas C et al.
Molecular Biology Reports, 2025
Dermoscopic furrow ink test of the palmar lesion in loricrin keratoderma.
Shirahama T et al.
The Journal of Dermatology, 2022
Palmoplantar keratoderma with honeycombing: A case of loricrin keratoderma with heterozygous frameshift mutation in LOR gene, from India.
Muna B et al.
Indian Journal of Dermatology, Venereology and Leprology, 0
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