De novo GRIN1 mutations: An emerging cause of severe early infantile encephalopathy

Autor: Zehavi, Yoav, Mandel, Hanna, Zehavi, Arie, Rashid, Muhammad Abu, Straussberg, Rachel, Jabur, Banan, Shaag, Avraham, Elpeleg, Orly, Spiegel, Ronen
Zdroj: In European Journal of Medical Genetics June 2017 60(6):317-320
Databáze: ScienceDirect