Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism
Eva Al Taji(Charles University), Heiko Krude(Humboldt-Universität zu Berlin), Annette Grüters(Unknown), Christof Dame, Heike Biebermann(Humboldt-Universität zu Berlin), O Hníková, Z Límanová(Charles University), Jaroslav Zikmund(Charles University), Jan Lebl(Charles University)
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