Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Xuqin Liang"'
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Familial renal glucosuria (FRG) is a rare genetic condition featured by isolated glucosuria without hyperglycemia or other kidney diseases. It is caused by pathogenic mutations of the SGLT2 (Sodium-Glucose Cotransporter 2) gene, whose protein product
Externí odkaz:
https://doaj.org/article/5af5892fe205408183710ac5f1c50a88
Autor:
Shujie Hou, Xuqin Liang, Yuhua Jiao, Boxi Yan, Kangying Liu, Hongmei Lin, Yi Ding, Huimei Huang, Jieni Zhang, Huaxiang Zhao
Publikováno v:
Journal of Clinical Pediatric Dentistry; Nov2024, Vol. 48 Issue 6, p1-11, 11p
Autor:
Huaxiang Zhao, Qing He, Xiantao Wu, Xuqin Liang, Yuhua Jiao, Yue Zhang, Shanying Bao, Linping Xu, Yuxia Hou, Xuechen Zhu, Yi Ding
Publikováno v:
Genomics. 115:110630
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::911e02a1d559723f12ab34f1e624b4ad
https://doi.org/10.1016/j.ygeno.2023.110630
https://doi.org/10.1016/j.ygeno.2023.110630