CDKN2A: The IVS2-105A/G Intronic Mutation Found in an Italian Patient Affected by Eight Primary Melanomas

Author:

Majore Silvia,Catricalà Caterina,Binni Francesco,Simone Paola De,Eibenschutz Laura,Grammatico Paola

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference15 articles.

1. MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations;Box;Am J Hum Genet,2001

2. CDKN2A mutations in melanoma;Dracopoli;Cancer Surv,1996

3. The genetics of hereditary melanoma and nevi;Greene;Cancer,1999

4. A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees;Harland;Hum Mol Genet,2001

5. CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas;Hashemi;Cancer Res,2000

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