eIF2B Modulators in Vanishing White Matter

eIF2B Modulators in Vanishing White Matter

Vanishing White Matter (VWM) disease is a rare and fatal leukodystrophy, caused by recessive mutations in the five genes encoding the protein complex eukaryotic translation initiation factor 2B (eIF2B). eIF2B plays a crucial role in initiating and regulating the...
Auditory Event-Related Potentials EEG-Recording in Fmr1 KO mice

Auditory Event-Related Potentials EEG-Recording in Fmr1 KO mice

July is Fragile X Syndrome (FXS) Awareness month, a time dedicated to raising awareness about this rare genetic disorder, affecting thousands of individuals worldwide. We are deeply committed to accelerating the availability of targeted therapies to improve the lives...
Auditory Event-Related Potentials EEG-Recording in Fmr1 KO mice

EEG Recording in the Epileptic Encephalopathy Model

September is STXBP1 disorders awareness month, an initiative aimed at raising awareness of STXBP1-related rare genetic disorders, such as epileptic encephalopathy. Although STXBP1-related disorders are rare; STXBP1 is the 5th most common cause of genetic forms of...