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CDKN2A variants in a population-based sample of Queensland families with melanoma.

Authors
Type
Published Article
Journal
JNCI Journal of the National Cancer Institute
0027-8874
Publisher
Oxford University Press
Publication Date
Volume
91
Issue
5
Pages
446–452
Identifiers
PMID: 10070944
Source
Medline

Abstract

CDKN2A mutations are rare in this population (approximately 0.2% of all melanoma cases in Queensland) and appear to be associated with melanoma in only the most affected families. The Nt500G allele appears to be associated with familial risk, but this association probably reflects Celtic ancestry.

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