Genetic Features of Chinese Patients with Gitelman Syndrome: Sixteen Novel SLC12A3 Mutations Identified in a New Cohort

Conclusion: < /i > < /b > Sixteen novel < i > SLC12A3 < /i > pathogenic mutations were identified in a cohort of Chinese patients with GS. T60M and D486N were most frequent and appear to be important candidate alleles in Chinese patients with GS. < br / > Am J Nephrol 2016;44:113-121
Source: American Journal of Nephrology - Category: Neurology Source Type: research