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
- Moya, C.M.
- De Nanclares, G.P.
- Castaño, L.
- Potau, N.
- Bilbao, J.R.
- Carrascosa, A.
- Bargadá, M.
- Coya, R.
- Martul, P.
- Vicens-Calvet, E.
- Santisteban, P.
ISSN: 0021-972X, 0021-972X
Année de publication: 2006
Volumen: 91
Número: 5
Pages: 1832-1841
Type: Article
