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.
Aldizkaria:
Journal of Clinical Endocrinology and Metabolism

ISSN: 0021-972X,  0021-972X

Argitalpen urtea: 2006

Alea: 91

Zenbakia: 5

Orrialdeak: 1832-1841

Mota: Artikulua

DOI: 10.1210/JC.2005-1497 GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus