Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy

Neurol India. 2016 Mar-Apr;64(2):327-8. doi: 10.4103/0028-3886.177628.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Cadherins / genetics*
  • Diagnosis, Differential
  • Epilepsies, Partial / diagnosis*
  • Epilepsy / diagnosis
  • Epilepsy / genetics*
  • Humans
  • Infant
  • Mutation
  • Protocadherins

Substances

  • Cadherins
  • PCDH19 protein, human
  • Protocadherins