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1Constitutively 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..
14 years ago by @pharmawuerz
show all tags
Methimazole/therapeutic
Agents/therapeutic
Humans
use
Male
Preschool
Infant
Child,
Germ-Line
Receptor
Point
Pedigree
DNA/analysis
Hyperthyroidism/*congenital/drug
therapy/*genetics
Adult
Mutation
Thyrotropin/*genetics
Antithyroid
Female
Methimazole/therapeuticAgents/therapeuticHumansuseMalePreschoolInfantChild,Germ-LineReceptorPointPedigreeDNA/analysisHyperthyroidism/*congenital/drugtherapy/*geneticsAdultMutationThyrotropin/*geneticsAntithyroidFemale
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