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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Huvudupphovsmän: PONTI, GIOVANNI, POLLIO, ANNAMARIA, PASTORINO, LORENZA, PELLACANI, GIOVANNI, MAGNONI, CRISTINA, NASTI, SABINA, FORTUNA, GIULIO, TOMASI, ALDO, SCARRÀ, GIOVANNA BIANCHI, SEIDENARI, STEFANIA
Materialtyp: Artigo
Språk:Inglês
Publicerad: D.A. Spandidos 2012
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Articles
Länkar: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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