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A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 5, p. 301, doi. 10.1038/jhg.2012.20
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- Publication type:
- Article
Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community.
- Published in:
- 2009
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- Publication type:
- journal article
Mosaicism of a Thyroid Hormone Receptor-β Gene Mutation in Resistance to Thyroid Hormone.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3471, doi. 10.1210/jc.2006-0727
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- Publication type:
- Article
A Novel Thyroid Hormone Receptor Beta Gene Mutation (G251V) in a Thai Patient with Resistance to Thyroid Hormone Coexisting with Pituitary Incidentaloma.
- Published in:
- Thyroid, 2016, v. 26, n. 12, p. 1804, doi. 10.1089/thy.2016.0450
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- Publication type:
- Article
Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.
- Published in:
- Clinical Endocrinology, 2007, v. 66, n. 5, p. 695, doi. 10.1111/j.1365-2265.2007.02804.x
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- Publication type:
- Article