QuickView for RAI1;jsessionid=34650181E17EE093969EC349E960E464 (gene)

1. Comparative analyses of the Smith-Magenis syndrome protein RAI1 in mice and common marmoset monkeys.
2. Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
3. Allele-Specific Regulation of the Candidate Autism Liability Gene RAI1 by the Enhancer Variant rs492…
4. Loss of Rai1 enhances hippocampal excitability and epileptogenesis in mouse models of Smith-Magenis …
5. Smith-Magenis syndrome protein RAI1 regulates body weight homeostasis through hypothalamic BDNF-prod…

There were no clinical trials for RAI1;jsessionid=34650181E17EE093969EC349E960E464