Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome-Reference-Cited by-同舟云学术

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Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome

Published:2022-12-28 Issue: Volume: Page:
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Ying Qiao¹^ORCID,Ye Zhinan²,Zhang Wei¹,Pan Yingying¹,Dai Linxiong¹,Lin Kaisang¹,Feng Xiaocheng³,Dong Xuehong³,He Fei¹^ORCID

Affiliation:

1. Department of Endocrinology and Metabolism Taizhou Municipal Hospital Taizhou Zhejiang People's Republic of China

2. Department of Neurology Taizhou Municipal Hospital Taizhou Zhejiang People's Republic of China

3. Department of Endocrinology and Metabolism, School of Medicine Zhejiang University Affiliated Sir Run Shaw Hospital Hangzhou Zhejiang People's Republic of China

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14870

Reference34 articles.

1. Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study

2. Gitelman syndrome

3. Heterozygous mutations of the sodium chloride cotransporter in Chinese children: prevalence and association with blood pressure

4. Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases;Kondo A;Sci Rep,2021

5. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

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