Art

J-GLOBAL ID：200902121142091180   Reference number：95A0209417

Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.

Author (9)： KOPP P (Univ. Bern, Bern, CHE) ,  VAN SANDE J (Univ. Brussels, Brussels, BEL) ,  PARMA J (Univ. Brussels, Brussels, BEL) ,  DUPREZ L (Univ. Brussels, Brussels, BEL) ,  GERBER H (Univ. Bern, Bern, CHE) ,  JOSS E (Univ. Bern, Bern, CHE) ,  JAMESON J L (Northwestern Univ., Chicago) ,  DUMONT J E (Univ. Brussels, Brussels, BEL) ,  VASSART G (Univ. Brussels, Brussels, BEL)
Material： New England Journal of Medicine  (N Engl J Med)
Volume： 332  Issue： 3  Page： 150-154  Publication year： Jan. 19, 1995 
JST Material Number： H0784A  ISSN： 0028-4793  CODEN： NEJMAG  Document type： Article
Country of issue： United States (USA)  Language： ENGLISH (EN)