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Article

Coincident two mutations and one single nucleotide polymorphism of the PTCH1 gene in a family with naevoid basal cell carcinoma syndrome.

Acta dermato-venereologica - 1 Jan 2008

Abe Shoko, Kabashima Kenji, Sakabe Junichi, Shimauchi Takatoshi, Yan Zhang, Okamoto Tetsuji, Tokura Yoshiki

Abstract excerpt

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Share to Aged
Share to Basal Cell Nevus Syndrome
Share to Child, Preschool
Share to Immunohistochemistry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Patched-1 Receptor

Share to Patched Receptors

Share to Polymorphism, Single Nucleotide

Share to Receptors, Cell Surface

Source

Identifiers

PMID: 19002359
DOI: 10.2340/00015555-0524

Genes

PTCH1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

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Coincident two mutations and one single nucleotide polymorphism of the PTCH1 gene in a family with naevoid basal cell carcinoma syndrome.PMID 19002359Read ↗

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Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.Semantic proximity Read ↗

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndromeSemantic proximity Read ↗

New mutation of the patched homologue 1 gene in a Chinese family with naevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features.Semantic proximity Read ↗

Characterisation of human patched germ line mutations in naevoid basal cell carcinoma syndromeSemantic proximity Read ↗

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