Absence of germlineCDKN2Amutation in Sicilian patients with familial malignant melanoma: Could it be a population-specific genetic signature?-Reference-Cited by-同舟云学术

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Absence of germlineCDKN2Amutation in Sicilian patients with familial malignant melanoma: Could it be a population-specific genetic signature?

Published:2015-12-09 Issue:1 Volume:17 Page:83-90
ISSN:1538-4047
Container-title:Cancer Biology & Therapy
language:en
Short-container-title:Cancer Biology & Therapy

Author:

Di Lorenzo Sara,Fanale Daniele,Corradino Bartolo,Caló Valentina,Rinaldi Gaetana,Bazan Viviana,Giordano Antonio,Cordova Adriana,Russo Antonio

Publisher

Informa UK Limited

Subject

Cancer Research,Pharmacology,Oncology,Molecular Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1080/15384047.2015.1108494

Reference69 articles.

1. Targeted Therapies in Melanoma

2. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group [published erratum appears in Hum Mol Genet 1998 May;7(5):941]

3. Melanoma and genetics

4. Malignant melanoma: genetics and therapeutics in the genomic era

5. Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus

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