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Gorlin-Goltz Syndrome

The Gorlin-Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome—NBCCS) is a rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene found on chromosome arm 9q. The syndrome, characterized by increased predisposition to develop basal cell carcinoma and associated...

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Autors principals: Pandeshwar, Padma, Jayanthi, K., Mahesh, D.
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2012
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3469076/
https://ncbi.nlm.nih.gov/pubmed/23082255
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/247239
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