Genetic variation and risk of chronic lymphocytic leukaemia.

Abstract:

:Chronic lymphocytic leukaemia (CLL) is the most common form of lymphoid malignancy in Western countries, accounting for around a quarter of all leukaemias. Evidence from epidemiological and family studies have provided evidence for familial clustering of CLL compatible with inherited genetic predisposition to CLL. Direct evidence for genetic susceptibility has been provided by a recent genome wide association study of CLL which has identified common variants at 10 different loci which influence CLL risk. Here we review the current knowledge regarding the allelic architecture of susceptibility to CLL and what the currently identified risk loci are telling us regarding disease aetiology.

journal_name

Semin Cancer Biol

authors

Crowther-Swanepoel D,Houlston RS

doi

10.1016/j.semcancer.2010.08.006

subject

Has Abstract

pub_date

2010-12-01 00:00:00

pages

363-9

issue

6

eissn

1044-579X

issn

1096-3650

pii

S1044-579X(10)00078-7

journal_volume

20

pub_type

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