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Splicing Characterization of CLCNKB Variants in Four Patients With Type III Bartter Syndrome

OBJECTIVE: Type III Bartter syndrome (BS) is caused by loss-of-function mutations in the gene encoding basolateral chloride channel ClC-Kb (CLCNKB), and is characterized by hypokalemic metabolic alkalosis and hyperreninemic hyperaldosteronism. Here, we investigated the molecular defects in four Chin...

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Detalles Bibliográficos
Autores principales:	Wang, Chunli, Han, Yuan, Zhou, Jiaran, Zheng, Bixia, Zhou, Wei, Bao, Huaying, Jia, Zhanjun, Zhang, Aihua, Huang, Songming, Ding, Guixia, Zhao, Fei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047732/ https://www.ncbi.nlm.nih.gov/pubmed/32153641 http://dx.doi.org/10.3389/fgene.2020.00081

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