Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations

作者:De Rubeis Silvia; Siper Paige M; Durkin Allison; Weissman Jordana; Muratet Francois; Halpern Danielle; Trelles Maria del Pilar; Frank Yitzchak; Lozano Reymundo; Wang A Ting; Holder J Lloyd Jr; Betancur Catalina; Buxbaum Joseph D; Kolevzon Alexander
来源:Molecular Autism, 2018, 9(1): 31.
DOI:10.1186/s13229-018-0205-9