PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study

The patched (PTCH) mutation rate in nevoid basal cell carcinoma syndrome (NBCCS) reported in various studies ranges from 40 to 80%. However, few studies have investigated the role of PTCH in clinical conditions suggesting an inherited predisposition to basal cell carcinoma (BCC), although it has bee...

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Detalles Bibliográficos
Autores principales: Soufir, N, Gerard, B, Portela, M, Brice, A, Liboutet, M, Saiag, P, Descamps, V, Kerob, D, Wolkenstein, P, Gorin, I, Lebbe, C, Dupin, N, Crickx, B, Basset-Seguin, N, Grandchamp, B
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Genetics and Genomics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360669/
https://www.ncbi.nlm.nih.gov/pubmed/16909134
http://dx.doi.org/10.1038/sj.bjc.6603303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360669/
https://www.ncbi.nlm.nih.gov/pubmed/16909134
http://dx.doi.org/10.1038/sj.bjc.6603303

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