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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Main Authors: PONTI, GIOVANNI, POLLIO, ANNAMARIA, PASTORINO, LORENZA, PELLACANI, GIOVANNI, MAGNONI, CRISTINA, NASTI, SABINA, FORTUNA, GIULIO, TOMASI, ALDO, SCARRÀ, GIOVANNA BIANCHI, SEIDENARI, STEFANIA
Formato: Artigo
Idioma:Inglês
Publicado: D.A. Spandidos 2012
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Articles
Acceso en liña: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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