Associated Papers
Gorlin-Like Phenotype in a Young Girl With a De Novo PTCH2 Variant Mutation of Uncertain Significance.
Garcia-Garcia M et al.
The American Journal of Dermatopathology, 2024
PTCH2 is not a strong candidate gene for gorlin syndrome predisposition.
Smith MJ et al.
Familial Cancer, 2022
A healthy individual with a homozygous PTCH2 frameshift variant: Are variants of PTCH2 associated with nevoid basal cell carcinoma syndrome?
Altaraihi M et al.
Human Genome Variation, 2019
Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.
Fujii K et al.
Familial Cancer, 2013
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