A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: A case report

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

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