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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Main Authors: 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.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Public Library of Science 2012
Ábhair:
Research Article
Rochtain Ar Líne: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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