Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder
全基因组测序揭示家族性自闭症谱系障碍中存在新生SHANK3突变
期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0116358
Nemirovsky, Sergio I; Córdoba, Marta; Zaiat, Jonathan J; Completa, Sabrina P; Vega, Patricia A; González-Morón, Dolores; Medina, Nancy M; Fabbro, Mónica; Romero, Soledad; Brun, Bianca; Revale, Santiago; Ogara, María Florencia; Pecci, Adali; Marti, Marcelo; Vazquez, Martin; Turjanski, Adrián; Kauffman, Marcelo A
