Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction

por Marco, Elysa Jill, Aitken, Anne Brandes, Nair, Vishnu Prakas, da Gente, Gilberto, Gerdes, Molly Rae, Bologlu, Leyla, Thomas, Sean, Sherr, Elliott H.
Publicado 2018