Loss-of-Function Variants in a Hungarian Cohort Reveal Structural Insights on TSH Receptor Maturation and Signaling

Context Congenital hypothyroidism (CH) is one of the most common inborn endocrine disorders with genetic background. Despite the well-established newborn CH screening program in Hungary, no systematic examination of the underlying genetic alterations has been performed yet. Objective We aimed to exp...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Lábadi Árpád
Grassi Elisa Stellaria
Gellén Balázs
Kleinau Gunnar
Biebermann Heike
Ruzsa Beáta
Gelmin Giulia
Rideg Orsolya
Miseta Attila János
Kovács L. Gábor
Patócs Attila Balázs
Felszeghy Enikő
Nagy Endre
Mezősi Emese
Persani Luca
Dokumentumtípus: Cikk
Megjelent: 2015
Sorozat:JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 100 No. 7
Tárgyszavak:
doi:10.1210/jc.2014-4511

mtmt:2894542
Online Access:http://publicatio.bibl.u-szeged.hu/27342

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