Vorschau von „Stogmann2013.pptx“ copy

Pedigree of the Egyptian family reported by Stogmann et al. Using homozygosity mapping and exome sequencing, they identified a mutation in CNTN2 in this family with cortical myoclonic tremor and epilepsy.

Ingo Helbig

Child Neurology Fellow and epilepsy genetics researcher at the Children’s Hospital of Philadelphia (CHOP), USA and Department of Neuropediatrics, Kiel, Germany

Facebook Twitter 

Leave a Reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.