Glycogen storage disease (GSD) type III (OMIM 232400) is due to glycogen debranching enzyme (GDE; EC 3.2.1.33) deficiency encoded by the AGL gene. The estimated incidence of the disease is estimated ...

A team of researchers has linked neuronal activity to the levels of sphingolipids, a type of fat, in brain cells. Furthermore, disruption of sphingolipid metabolism led to significant neuronal damage ...