Lack of association between polymorphisms in the UBASH3A gene and autoimmune thyroid disease: A case control study;Falta de associação entre polimorfismos do gene UBASH3A e doença tiroidiana autoimune: Estudo caso controle

Arquivos Brasileiros de Endocrinologia e Metabologia

Volumn 58, Issue 6, 2014, Pages 640-645

  Cai, Tian Tian ^a   Wang, Xuan ^a   Muhali, Fatuma Said ^a   Song, Rong Hua ^a   Shi, Xiao Hong ^b   Jiang, Wenjuan ^b   Xiao, Ling ^b   Li, Dan Feng ^b   Zhang, Jin An ^b  

^a XI'AN JIAOTONG UNIVERSITY   (China)

^b JINSHAN HOSPITAL OF FUDAN UNIVERSITY   (China)

Author keywords

Autoimmune thyroid disease (AITD); Graves disease (GD); Hashimoto s thyroiditis (HT); Single nucleotide polymorphism (SNP); Ubiquitin associated and SH3 domain containing A (UBASH3A)

Indexed keywords

SIGNAL TRANSDUCING ADAPTOR PROTEIN; UBASH3A PROTEIN, HUMAN;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CASE CONTROL STUDY; CHILD; CHINA; ENDOCRINE OPHTHALMOPATHY; ETHNOLOGY; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; HAPLOTYPE; HASHIMOTO DISEASE; HUMAN; IMMUNOLOGY; MALE; MASS SPECTROMETRY; MIDDLE AGED; PRESCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; YOUNG ADULT;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CHINA; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; GRAVES OPHTHALMOPATHY; HAPLOTYPES; HASHIMOTO DISEASE; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; YOUNG ADULT;

EID: 84907007954     PISSN: 00042730     EISSN: 16779487     Source Type: Journal    
DOI: 10.1590/0004-2730000003209     Document Type: Article

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