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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Impact Journals LLC
2017
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| Materias: | |
| 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 |