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February 28, 2006The Journal of Clinical Endocrinology & MetabolismOpen Access

Functional Study of a Novel Single Deletion in theTITF1/NKX2.1Homeobox Gene That Produces Congenital Hypothyroidism and Benign Chorea But Not Pulmonary Distress

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Authors

CMChristian M. MoyaGNGuiomar Pérez de NanclaresLCLuís Castaño

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Moya et al. (2006) studied this question.

synapsesocial.com/papers/6a0d2e4a48a82a5ce309a83dhttps://doi.org/10.1210/jc.2005-1497
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