CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report

por Tolmacheva, Ekaterina R., Shubina, Jekaterina, Kochetkova, Taisiya O., Ushakova, Lubov’ V., Bokerija, Ekaterina L., Vasiliev, Grigory S., Mikhaylovskaya, Galina V., Atapina, Ekaterina E., Zaretskaya, Nadezhda V., Sukhikh, Gennady T., Rebrikov, Denis V., Trofimov, Dmitriy Yu.
Publicado 2023