Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress

  1. Moya, C.M.
  2. De Nanclares, G.P.
  3. Castaño, L.
  4. Potau, N.
  5. Bilbao, J.R.
  6. Carrascosa, A.
  7. Bargadá, M.
  8. Coya, R.
  9. Martul, P.
  10. Vicens-Calvet, E.
  11. Santisteban, P.
Journal:
Journal of Clinical Endocrinology and Metabolism

ISSN: 0021-972X,  0021-972X

Year of publication: 2006

Volume: 91

Issue: 5

Pages: 1832-1841

Type: Article

DOI: 10.1210/JC.2005-1497 GOOGLE SCHOLAR lock_openOpen access editor
Data source: Scopus