Genetic variants in mannose receptor gene (MRC1) confer susceptibility to increased risk of sarcoidosis

BMC Medical Genetics

Volumn 11, Issue 1, 2010, Pages

  Hattori, Takeshi ^a   Konno, Satoshi ^a   Takahashi, Ayumu ^a   Isada, Akira ^a   Shimizu, Kaoruko ^a   Shimizu, Kenichi ^a   Taniguchi, Natsuko ^a   Gao, Peisong ^b   Yamaguchi, Etsuro ^c   Hizawa, Nobuyuki ^d   Huang, Shau Ku ^b   Nishimura, Masaharu ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b JOHNS HOPKINS ASTHMA AND ALLERGY CENTER   (United States)

^c AICHI MEDICAL UNIVERSITY   (Japan)

^d UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MANNOSE RECEPTOR;

3' UNTRANSLATED REGION; ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CONTROLLED STUDY; DISEASE COURSE; EXON; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HUMAN; INTRON; JAPANESE; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; SARCOIDOSIS; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; CASE CONTROL STUDY; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED;

ADOLESCENT; ADULT; AGED; CASE-CONTROL STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; SARCOIDOSIS;

EID: 77958556482     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-11-151     Document Type: Article

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