Partial deficiency of Thyroid transcription factor 1 produces predominantly neurological defects in humans and mice

Three genes, TTF1, TTF2, and PAX8, involved in thyroid gland development and migration have been identified. Yet systematic screening for defects in these genes in thyroid dysgenesis gave essentially negative results. In particular, no TTF1 gene defects were found in 76 individuals with thyroid dysg...

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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Pohlenz, Joachim, Dumitrescu, Alexandra, Zundel, Dorothee, Martiné, Ursula, Schönberger, Winfried, Koo, Eugene, Weiss, Roy E., Cohen, Ronald N., Kimura, Shioko, Refetoff, Samuel
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 2002
Assuntos:	Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC150877/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11854318/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI14192
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