Mutation spectrum of Chinese patients with Bartter syndrome

OBJECTIVE: Bartter syndrome (BS) has been rarely reported in Chinese population except for a few case reports. This investigation was aimed to analyze the mutations of the causal genes in sixteen Chinese patients with BS, and review their followup and treatment. METHODS: Identify mutations by the ne...

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Detalles Bibliográficos
Autores principales: Han, Yue, Lin, Yi, Sun, Qing, Wang, Shujuan, Gao, Yanxia, Shao, Leping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731900/
https://www.ncbi.nlm.nih.gov/pubmed/29254190
http://dx.doi.org/10.18632/oncotarget.21355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731900/
https://www.ncbi.nlm.nih.gov/pubmed/29254190
http://dx.doi.org/10.18632/oncotarget.21355

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