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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532205/
https://www.ncbi.nlm.nih.gov/pubmed/23285148
http://dx.doi.org/10.1371/journal.pone.0052685

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532205/
https://www.ncbi.nlm.nih.gov/pubmed/23285148
http://dx.doi.org/10.1371/journal.pone.0052685

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