Clinical exome sequencing identifies two novel IQSEC2 mutations associated with X-linked intellectual disability with seizures: implications for genetic counseling and clinical diagnosis
Authors: S. Tang; S.K. Gandomi; K.D. Farwell Gonzalez; L. Shahmirzadi; J. Mancuso; P. Pichurin; R. Temme; S. Dugan; W. Zeng
Collaborators: Children's Hospital and Clinics of Minnesota; Mayo Clinic