Association of single nucleotide polymorphism rs3792876 in SLC22A4 gene with autoimmune thyroid disease in a Chinese Han population

BMC Medical Genetics

Volumn 16, Issue 1, 2015, Pages

  Hou, Xin ^a,b   Mao, Jinyuan ^b   Li, Yushu ^a,b   Li, Jia ^b   Wang, Weiwei ^a,b   Fan, Chenling ^b   Wang, Hong ^b   Zhang, Hongmei ^b   Shan, Zhongyan ^a,b   Teng, Weiping ^a,b  

^a CHINA MEDICAL UNIVERSITY   (China)

^b Key Laboratory of Endocrine Diseases ^*  (China)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE TRANSPORTER 1; ORGANIC CATION TRANSPORTER; SLC22A4 PROTEIN, HUMAN;

ADULT; ARTICLE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPING TECHNIQUE; GRAVES DISEASE; HAN CHINESE; HASHIMOTO DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; SINGLE NUCLEOTIDE POLYMORPHISM; SLC22A4 GENE; ASIAN CONTINENTAL ANCESTRY GROUP; AUTOIMMUNE DISEASE; ETHNOLOGY; GENETICS; THYROID DISEASE;

ASIAN CONTINENTAL ANCESTRY GROUP; AUTOIMMUNE DISEASES; GENOTYPING TECHNIQUES; HUMANS; ORGANIC CATION TRANSPORT PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; THYROID DISEASES;

EID: 84940506879     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/s12881-015-0222-x     Document Type: Article

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