Novel Patched 1 mutations in patients with nevoid basal cell carcinoma syndrome – case report

Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is a rare autosomal dominant disorder characterized by numerous basal cell carcinomas, keratocystic odontogenic tumors of the jaws, and diverse developmental defects. This disorder is associated with mutations in tumor suppressor gene Patched 1...

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Detalles Bibliográficos
Autores principales: Škodrić-Trifunović, Vesna, Stjepanović, Mihailo, Savić, Živorad, Ilić, Miroslav, Kavečan, Ivana, Jovanović Privrodski, Jadranka, Spasovski, Vesna, Stojiljković, Maja, Pavlović, Sonja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Medical Schools 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364350/
https://www.ncbi.nlm.nih.gov/pubmed/25727044
http://dx.doi.org/10.3325/cmj.2015.56.63

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364350/
https://www.ncbi.nlm.nih.gov/pubmed/25727044
http://dx.doi.org/10.3325/cmj.2015.56.63

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