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.

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

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