Clinical features of pediatric renal glucosuria cases due to SLC5A2 gene variants-Reference-Cited by-同舟云学术

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Clinical features of pediatric renal glucosuria cases due to SLC5A2 gene variants

Published:2021-08-11 Issue: Volume: Page:
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:Pediatrics International

Author:

Dorum Sevil¹^ORCID,Erdoğan Hakan²^ORCID,Köksoy Adem Yasin³,Topak Ali⁴,Görükmez Özlem⁴

Affiliation:

1. Medical Doctor Department of Pediatrics Division of Metabolism Bursa Yuksek Ihtisas Training and Research Hospital Bursa Turkey

2. Professor, Department of Pediatrics Division of Nephrology Bursa Yuksek Ihtisas Training and Research Hospital Bursa Turkey

3. Medical Doctor Department of Pediatrics Division of Nephrology Van Training and Research Hospital Van Turkey

4. Medical Doctor Department of Genetics Bursa Yuksek Ihtisas Training and Research Hospital Bursa Turkey

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ped.14948

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial renal glycosuria identified in an Indian family;BMJ Case Reports;2024-09

2. Sodium-iodide symporter and its related solute carriers in thyroid cancer;Journal of Endocrinology;2024-02-08

3. Performance of the ACMG‐AMP criteria in a large familial renal glucosuria cohort with identified SLC5A2 sequence variants;Clinical Genetics;2023-06-22

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