Arquivo
IDENTIFICATION OF NOVEL GENETIC CAUSES OF RETT SYNDROME-LIKE PHENOTYPES BY WHOLE EXOME SEQUENCING
Lopes F1, Barbosa M2, Ameur A3, Soares G4, de Sá J5, Dias Ana Isabel6, Oliveira G7, Cabral P8, Temudo T9, Calado Eulália6, Cruz IF10, Vieira José Pedro6, Oliveira R5, Esteves S1,Sauer S11, Jonasson I3, Syvänen AC12, Gyllensten U3, Pinto D13, Maciel P1