2004;53:S1621
A DACP, Lopes C
KH: Investigation, Writing original draft, Writing review & editing, Formal analysis, Validation
Additionally, they play a vital role in heme synthesis, which is indispensable for oxygen transport and metabolism
Moreover, as multiple DNA regions can be mutated within the same gene, it is likely that the SCN1A mutation can be identified in multiple kinds of genetic epilepsies, including severe myoclonic epilepsy of infancy, epilepsy with febrile seizures plus, and partial epilepsy with febrile seizures plus
Indeed, clinical trials with FGF-21 analog monotherapy (e.g., pegbelfermin, efruxifermin, and BOS-580) have generated favorable results in NAFLD, as elsewhere summarized [52]