TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5. (Q42482160)
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scientific article published on August 2005
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5. |
scientific article published on August 2005 |
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TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5. (English)
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Beate Karges
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Gerd Krause
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Janos Homoki
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Wolfram Karges
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1 August 2005
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