Cargando…
Genetic Analysis of SLC12A3 Gene in Chinese Patients with Gitelman Syndrome
BACKGROUND: The incidence of Gitelman syndrome (GS) has been increasing in our hospital. The aim of this study was to explore the diagnostic accuracy and features of SLC12A3 gene in Chinese patients with GS. MATERIAL/METHODS: We searched the literature about Chinese patients with GS in the PubMed da...
Autores principales: | Zeng, Yanmei, Li, Ping, Fang, Shu, Wu, Chunyan, Zhang, Yudan, Lin, Xiaochun, Guan, Meiping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6703089/ https://www.ncbi.nlm.nih.gov/pubmed/31398183 http://dx.doi.org/10.12659/MSM.916069 |
Ejemplares similares
-
Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome
por: Kong, Yuanmei, et al.
Publicado: (2019) -
Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome
por: Lee, Jae Wook, et al.
Publicado: (2016) -
Correction to: Digenic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome
por: Kong, Yuanmei, et al.
Publicado: (2019) -
A novel mutation of SLC12A3 gene causing Gitelman syndrome
por: De Silva, Neomal, et al.
Publicado: (2022) -
Novel Intronic Mutations of the SLC12A3 Gene in Patients with Gitelman Syndrome
por: Xun, Zeli, et al.
Publicado: (2023)