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

Christian M. Moya, Guiomar Perez De Nanclares, Luis Castaño, Neus Potau, J. Ramón Bilbao, Antonio Carrascosa, María Bargadá, Raquel Coya, Pedro Martul, Enric Vicens-Calvet, Pilar Santisteban

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