Common variation at 12q24.13 (OAS3) influences chronic lymphocytic leukemia risk

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Bibliographic Details
Published in:	Leukemia Vol. 29; no. 3; pp. 748 - 751
Main Authors:	Sava, G P, Speedy, H E, Di Bernardo, M C, Dyer, M J S, Holroyd, A, Sunter, N J, Marr, H, Mansouri, L, Deaglio, S, Karabon, L, Frydecka, I, Jamroziak, K, Woszczyk, D, Juliusson, G, Smedby, K E, Jayne, S, Majid, A, Wang, Y, Dearden, C, Hall, A G, Mainou-Fowler, T, Jackson, G H, Summerfield, G, Harris, R J, Pettitt, A R, Allsup, D J, Bailey, J R, Pratt, G, Pepper, C, Fegan, C, Rosenquist, R, Catovsky, D, Allan, J M, Houlston, R S
Format:	Journal Article
Language:	English
Published:	London Nature Publishing Group UK 01-03-2015 Nature Publishing Group
Subjects:	2',5'-Oligoadenylate Synthetase - genetics 45/43 631/208 631/67/68 Alleles Cancer and Oncology Cancer och onkologi Cancer Research Case-Control Studies Chromosome Mapping Chromosomes, Human, Pair 12 - chemistry Chronic lymphocytic leukemia Clinical Medicine Critical Care Medicine Gene Frequency Genetic aspects Genetic Loci Genetic Predisposition to Disease Genetic variation Genome-Wide Association Study Health aspects Hematology Humans Identification and classification Intensive Internal Medicine Introns Klinisk medicin Letter to the Editor Leukemia, Lymphocytic, Chronic, B-Cell - genetics Leukemia, Lymphocytic, Chronic, B-Cell - pathology Medical and Health Sciences Medicin och hälsovetenskap Medicine Medicine & Public Health Odds Ratio Oncology Polymorphism, Single Nucleotide Risk Risk factors United Kingdom
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Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0887-6924 1476-5551 1476-5551
DOI:	10.1038/leu.2014.311