[16p11.2 microdeletion associated to early onset benign childhood seizures]

Rev Neurol. 2013 Jan 16;56(2):125-7.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 16 / genetics*
  • Humans
  • Infant
  • Language Development Disorders / genetics*
  • Male
  • Motor Skills Disorders / genetics*
  • Seizures / genetics*
  • Syndrome