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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Detalhes bibliográficos
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.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Research Article
Acesso em linha: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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