Constitutively active germline mutation of the thyrotropin receptor
gene as a cause of congenital hyperthyroidism
K. Schwab, M. Gerlich, M. Broecker, P. Sohlemann, M. Derwahl, and M. Lohse. J Pediatr, 131 (6):
899-904(December 1997)Schwab, K O Gerlich, M Broecker, M Sohlemann, P Derwahl, M Lohse,
M J Case Reports Research Support, Non-U.S. Gov't United states The
Journal of pediatrics J Pediatr. 1997 Dec;131(6):899-904..
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