Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts. [electronic resource]
Producer: 20110427Description: e15512 p. digitalISSN:- 1932-6203
- Case-Control Studies
- Cohort Studies
- Female
- Gene Frequency
- Genetic Predisposition to Disease -- genetics
- Genotype
- Graves Disease -- ethnology
- Haplotypes
- Humans
- Introns -- genetics
- Linkage Disequilibrium
- Logistic Models
- Male
- Poland
- Polymorphism, Single Nucleotide
- Receptors, Thyrotropin -- genetics
- Risk Factors
- United Kingdom
- White People -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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