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Article

Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis.

Anais brasileiros de dermatologia - 1 Jan 2019

Miyashiro Denis, Torezan Luis Antonio, Grinblat Beni Moreinas, Festa Neto Cyro

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Share to Basal Cell Nevus Syndrome
Share to Hedgehog Proteins
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Share to Patched-1 Receptor

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 31644632
DOI: 10.1590/abd1806-4841.20197449
PMCID: PMC7007026

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Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis.PMID 31644632Read ↗

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Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations.Semantic proximity Read ↗

New mutations and an updated database for the patched-1 (PTCH1) gene.Semantic proximity Read ↗

Germline PTCH1 mutations in Japanese basal cell nevus syndrome patients.Semantic proximity Read ↗

Inherited rare and common variants in PTCH1 and PTCH2 contributing to the predisposition to reproductive cancers.Semantic proximity Read ↗

A novel mutation of the PTCH1 gene activates the Shh/Gli signaling pathway in a Chinese family with nevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

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PTCH mutations: distribution and analyses.Semantic proximity Read ↗

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