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      Subclinical nonautoimmune hyperthyroidism in a family segregates with a thyrotropin receptor mutation with weakly increased constitutive activity.

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          Abstract

          Subclinical hyperthyroidism is usually associated with Graves' disease or toxic nodular goiter. Here we report a family with hereditary subclinical hyperthyroidism caused by a constitutively activating germline mutation of the thyrotropin receptor (TSHR) gene.

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          Author and article information

          Journal
          Thyroid
          Thyroid : official journal of the American Thyroid Association
          Mary Ann Liebert Inc
          1557-9077
          1050-7256
          Nov 2010
          : 20
          : 11
          Affiliations
          [1 ] Center for Excellence in Thyroid Care, Kuma Hospital, Kobe, Japan. nishihara@kuma-h.or.jp
          Article
          10.1089/thy.2010.0261
          2974847
          20929407
          b9982344-5c13-4c30-a643-8b6a63f0f87c
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