Exome sequencing identifies five mutations in the DYNC1H1 gene associated with severe neurological phenotypes
Authors: Stephanie K. Gandomi; Kelly D. Gonzalez; Dana Craiu; Johannes Lemke; Julie Cohen; Layla Shahmirzadi; Ira Lu; Sha Tang; Brigette Tippin Davis; Wenqi Zeng; Elizabeth Chao
Collaborators: EuroEPINOMICS, European Science Foundation; Inselspital University Hospital Bern; Kennedy Krieger Institute