Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report

Mutations in the Patched homolog 1 (PTCH1) gene lead to an autosomal dominant disorder known as nevoid basal cell carcinoma syndrome (NBCCS) or Gorlin syndrome (GS). Several PTCH1 mutations have been observed in NBCCS associated with keratocystic odontogenic tumors (KCOTs), including non-syndromic K...

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Autors principals: PONTI, GIOVANNI, POLLIO, ANNAMARIA, PASTORINO, LORENZA, PELLACANI, GIOVANNI, MAGNONI, CRISTINA, NASTI, SABINA, FORTUNA, GIULIO, TOMASI, ALDO, SCARRÀ, GIOVANNA BIANCHI, SEIDENARI, STEFANIA
Format: Artigo
Idioma:Inglês
Publicat: D.A. Spandidos 2012
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Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3402755/
https://ncbi.nlm.nih.gov/pubmed/22844361
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2012.707
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