Structure-function analysis of the glucose-6-phosphate transporter deficient in glycogen storage disease type Ib
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/11/25/3199/1552505/ddf312.pdf
Cited by 49 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. Clinical spectrum, over 12-year follow-up and experience of SGLT2 inhibitors treatment on patients with glycogen storage disease type Ib: a single-center retrospective study;Orphanet Journal of Rare Diseases;2024-04-11
2. Gene therapy and genome editing for type I glycogen storage diseases;Frontiers in Molecular Medicine;2023-03-31
3. Modifiable factors affecting renal preservation in type I glycogen storage disease after liver transplantation: a single-center propensity-match cohort study;Orphanet Journal of Rare Diseases;2021-10-11
4. SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation;Molecular Genetics and Metabolism Reports;2020-12
5. Glycogen storage disease type Ib: role of glucose‐6‐phosphate transporter in cell metabolism and function;FEBS Letters;2019-11-22
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