Meta-Analysis Combining New and Existing Data Sets Confirms that the TERT-CLPTM1L Locus Influences Melanoma Risk

被引：37

作者：

Law, Matthew H. ^{[1
]}

Montgomery, Grant W. ^{[1
]}

Brown, Kevin M. ^{[2
]}

Martin, Nicholas G. ^{[1
]}

Mann, Graham J. ^{[3
,4
]}

Hayward, Nicholas K. ^{[1
]}

MacGregor, Stuart ^{[1
]}

机构：

[1] Queensland Inst Med Res, Brisbane, Qld 4006, Australia

[2] NCI, Lab Translat Genom, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA

[3] Univ Sydney, Westmead Inst Canc Res, Millennium Inst, Westmead, NSW 2145, Australia

[4] Melanoma Inst Australia, Westmead, NSW, Australia

来源：

JOURNAL OF INVESTIGATIVE DERMATOLOGY | 2012年 / 132卷 / 02期

基金：

英国惠康基金;

关键词：

GENOME-WIDE ASSOCIATION; TELOMERE LENGTH; CANCER-RISK; SUSCEPTIBILITY; VARIANTS; SEQUENCE; DESIGN; CELLS; TERT; LINE;

D O I：

10.1038/jid.2011.322

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：485 / 487

页数：4

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