Multidisciplinary Approach for Mapping Genetic Variants in Naevoid Basal Cell Carcinoma Syndrome. Newly Identified Patched 1 Mutations in Half-Sisters
E. Vetró, J. Olah, T. Kalmar, Z. Maróti, E. Horvath, M. Szell, J. Piffko & L. Seres · Asian Journal of Dental Sciences · 2022
Objective: Naevoid basal cell carcinoma syndrome is a rare and autosomal dominant inherited condition with variable expressivity. Several genetic mutations have been identified but clear genotype-phenotype correlations have not been demonstrated; therefore, the diagnosis is still...
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Research Article