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TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5
Karges, B et al. (2005)
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UKU. Klinik für Innere Medizin I (1)
UKU. Klinik für Kinder- und Jugendmedizin (1)Personde Roux, N (1)
Debatin, Klaus-Michael (1)
Homoki, J (1)... View MoreResource typeWissenschaftlicher Artikel (1)Issue date
2005 (1)
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