Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism
- 1 December 1997
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 131 (6) , 899-904
- https://doi.org/10.1016/s0022-3476(97)70040-4
Abstract
No abstract availableKeywords
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