CASK mutation identified by whole exome sequencing in a patient that expands the clinical spectrum for MICPCH syndrome

• Title: CASK mutation identified by whole exome sequencing in a patient that expands the clinical spectrum for MICPCH syndrome
• Authors: J Zhao; S Tang; D Schuessler; N Dosa; RR Lebel
• Collaborators: SUNY Upstate Medical University, Syracuse, NY
• Conference: ASHG 2015
• Date: Tuesday, Oct 06, 2015 12:00am - 12:00pm