Risk of non-Hodgkin lymphoma in association with germline variation in complement genes

British Journal of Haematology

Volumn 145, Issue 5, 2009, Pages 614-623

  Cerhan, James R ^a,e   Novak, Anne J ^b   Fredericksen, Zachary S ^a   Wang, Alice H ^a   Liebow, Mark ^c   Call, Timothy G ^b   Dogan, Ahmet ^d   Witzig, Thomas E ^b   Ansell, Stephen M ^b   Habermann, Thomas M ^b   Kay, Neil E ^b   Slager, Susan L ^a  

^a Department of Health Sciences Research ^*

^b Division of Haematology   (Turkey)

^c Divisions of General Internal Medicine   (United States)

^d Mayo Clinic   (United States)

^e MAYO CLINIC   (United States)

Author keywords

Complement genes; Epidemiology; Genetic variation; Non Hodgkin lymphoma

Indexed keywords

ARTICLE; CANCER RISK; CONTROLLED STUDY; FEMALE; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NONHODGKIN LYMPHOMA; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; CHROMOSOME MAPPING; COMPLEMENT C5; COMPLEMENT C9; COMPLEMENT SYSTEM PROTEINS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GERM-LINE MUTATION; HAPLOTYPES; HUMANS; LOGISTIC MODELS; LYMPHOMA, NON-HODGKIN; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PRINCIPAL COMPONENT ANALYSIS; RISK ASSESSMENT; TNF RECEPTOR-ASSOCIATED FACTOR 1;

EID: 66149167461     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2009.07675.x     Document Type: Article

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