Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease.

Campbell, Purdey; Brix, Thomas H; Wilson, Scott G; Ward, Lynley C; Hui, Jennie; Beilby, John P; Hegedüs, Laszlo; Walsh, John P

Campbell, Purdey; Brix, Thomas H; Wilson, Scott G; Ward, Lynley C; Hui, Jennie; Beilby, John P; Hegedüs, Laszlo; Walsh, John P.

Afiliación

Campbell P; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Australia.
Brix TH; Department of Endocrinology and Metabolism, Odense University Hospital, Odense, Denmark.
Wilson SG; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Australia.
Ward LC; School of Medicine and Pharmacology, University of Western Australia, Crawley, Australia.
Hui J; Department of Twin Research and Genetic Epidemiology, King's College London, London, UK.
Beilby JP; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Australia.
Hegedüs L; Pathwest Laboratory Medicine WA, Nedlands, WA, Australia.
Walsh JP; Pathwest Laboratory Medicine WA, Nedlands, WA, Australia.

Clin Endocrinol (Oxf) ; 84(2): 278-283, 2016 Feb.

Article en En | MEDLINE | ID: mdl-25683181

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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Etiology_studies / Risk_factors_studies Idioma: En Revista: Clin Endocrinol (Oxf) Año: 2016 Tipo del documento: Article País de afiliación: Australia

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