The Ambiguous Role of NKX2-5 Mutations in Thyroid Dysgenesis

NKX2-5 is a homeodomain-containing transcription factor implied in both heart and thyroid development. Numerous mutations in NKX2-5 have been reported in individuals with congenital heart disease (CHD), but recently a select few have been associated with thyroid dysgenesis, among which the p.A119S v...

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Autors principals: van Engelen, Klaartje, Mommersteeg, Mathilda T. M., Baars, Marieke J. H., Lam, Jan, Ilgun, Aho, van Trotsenburg, A. S. Paul, Smets, Anne M. J. B., Christoffels, Vincent M., Mulder, Barbara J. M., Postma, Alex V.
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2012
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3532205/
https://ncbi.nlm.nih.gov/pubmed/23285148
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0052685
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