Compound Heterozygous and Homozygous Mutations of the TSHβ Gene as a Cause of Congenital Central Hypothyroidism in Europe

Publisher： Karger

E-ISSN： 1663-2826|62|3|149-155

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.62, Iss.3, 2004-09, pp. : 149-155

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