Glycogen storage disease type 1 due to SLC37A4 mutation

Any glycogen storage disease due to glucose-6-phosphatase deficiency in which the cause of the disease is a mutation in the SLC37A4 gene.

Also known as: G6P translocase deficiency, SLC37A4 glycogen storage disease I, glucose-6-phosphate translocase deficiency, glycogen storage disease I caused by mutation in SLC37A4

4 clinical trials for this condition and its sub-types, 0 tagged with Glycogen storage disease type 1 due to SLC37A4 mutation itself.