Logo

Beyond the Ion Channel

Understanding Epilepsy Genetics

Menu

Skip to content
  • Home
  • About this blog
  • The Epilepsiome
    • ALG13
    • ALDH7A1
    • ARX
    • ATP1A3
    • CACNA1A
    • CACNA1H
    • CDKL5
    • CHD2
    • DEPDC5
    • DNM1
    • FOXG1
    • GABRA1
    • GABRB3
    • GRIN2A
    • KCNQ2
    • KCNT1
    • LGI1
    • MECP2
    • PCDH19
    • PRRT2
    • PURA
    • Ring Chromosome 20
    • SCN1A
    • SCN2A
    • SCN8A
    • SLC2A1
    • SLC6A1
    • STXBP1
    • SYNGAP1
    • TBC1D24
    • WDR45
  • Teaching resources
  • The Beach Series Archive
  • Evidence & Interpretation

Tag Archives: P2N Kiel

The Biobank Dilemma

Posted on November 20, 2012 by Ingo Helbig (Kiel)

Killing two birds with one stone. I am currently preparing for a presentation for the Scientific Advisory Board of our local biobank network P2N and I thought that I wanted to share a few thoughts on biobanking and sample collection for epilepsy genetics that have troubled me for a while. Continue reading →

Posted in 2012, Bioethics, Epileptic encephalopathy, EuroEPINOMICS, Ideas
follow @ingohelbig


Tag Cloud

16p13.11 autism autosomal recessive disorders CACNA1A CDKL5 CHD2 ClinGen CNV de novo mutations DEPDC5 Dravet Syndrome Epi4K epilepsy epilepsy genetics epilepsy research epileptic encephalopathy EuroEPINOMICS exome exome sequencing febrile seizures GABRA1 GABRG2 GEFS+ genetic architecture genome sequencing GRIN2A GWAS Idiopathic Generalized Epilepsy Infantile Spasms intellectual disability juvenile myoclonic epilepsy KCNQ2 KCNT1 microdeletion precision medicine rare variants science SCN1A SCN1B SCN2A SCN8A STXBP1 SYNGAP1 whole exome sequencing whole genome sequencing

Subscribe to blog

Enter your email address to subscribe and receive notifications of new posts.

-------------------------------------------------

Archives

Categories

Meta

  • Log in
  • Entries feed
  • Comments feed
  • WordPress.org