Isolated Central Hypothyroidism in Young Siblings as a Manifestation of PROP1 Deficiency: Clinical Impact of Whole Exome Sequencing

Publisher： Karger

E-ISSN： 1663-2826|79|6|379-386

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.79, Iss.6, 2013-05, pp. : 379-386

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