The Role of KCNQ1 Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome

OBJECTIVE: Two missense mutations in KCNQ1, 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 so...

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Detalles Bibliográficos
Autores principales: Huttunen, Heta, Hero, Matti, Lääperi, Mitja, Känsäkoski, Johanna, Swan, Heikki, Hirsch, Joel A., Miettinen, Päivi J., Raivio, Taneli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928157/
https://www.ncbi.nlm.nih.gov/pubmed/29740400
http://dx.doi.org/10.3389/fendo.2018.00194

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928157/
https://www.ncbi.nlm.nih.gov/pubmed/29740400
http://dx.doi.org/10.3389/fendo.2018.00194

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