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Pubmed ID :29740400
Publication Date : //

The Role of Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome.


Two missense mutations in , an imprinted gene that encodes the alpha subunit of the voltage-gated potassium channel Kv7.1, cause autosomal dominant growth hormone deficiency and maternally inherited gingival fibromatosis. We evaluated endocrine features, birth size, and subsequent somatic growth of patients with long QT syndrome 1 (LQT1) due to loss-of-function mutations in .

Authors : Huttunen Heta , Hero Matti , Lääperi Mitja , Känsäkoski Johanna , Swan Heikki , Hirsch Joel A , Miettinen Päivi J , Raivio Taneli ,

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