Loading...
Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome
Gitelman's syndrome (GS) is caused by loss-of-function mutations in SLC12A3 and characterized by hypokalemic metabolic alkalosis, hypocalciuria, and hypomagnesemia. Long-term prognosis and the role of gene diagnosis in GS are still unclear. To investigate genotype-phenotype correlation in GS an...
Na minha lista:
| Udgivet i: | J Korean Med Sci |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
The Korean Academy of Medical Sciences
2016
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4712579/ https://ncbi.nlm.nih.gov/pubmed/26770037 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2016.31.1.47 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|