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A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report by Y. Watanabe, E. Sharwood, B. Goodwin, M. K. Creech, H. Y. Hassan, M. G. Netea, M. Jaeger, A. Dumitrescu, S. Refetoff, T. Huynh, R. E. Weiss
Published 2018Connect to this object online.
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