Variable Clinical Phenotypes in a Family with Homozygous c.1159G>A Mutation in the Thyroid Peroxidase Gene

Publisher： Karger

E-ISSN： 1663-2826|81|5|356-360

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.81, Iss.5, 2014-04, pp. : 356-360

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