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Gorlin syndrome: A rare case report
Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. The syndrome is caused by mutations in PTCH, a tumor suppressor gene that has been mapped to chromosome 9q22.3-q31. It is observed that most aggressive forms of keratocystic odontoge...
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| Publicado no: | J Oral Maxillofac Pathol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8083426/ https://ncbi.nlm.nih.gov/pubmed/33967525 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0973-029X.190048 |
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