Huda Zoghbi

Neuron. 2016 Oct 19;92(2):287-289. doi: 10.1016/j.neuron.2016.10.013. Epub 2016 Oct 19.

Abstract

Huda Zoghbi's experience diagnosing patients with Rett syndrome motivated her scientific research. In an interview with Neuron, she shares a trinucleotide repeat expansion discovery story, offers advice for young investigators, and discusses the tools needed to drive discovery forward.

Publication types

  • Interview

MeSH terms

  • Biomedical Research*
  • Humans
  • Interdisciplinary Communication
  • Mental Retardation, X-Linked / genetics
  • Neurology*
  • Rett Syndrome / genetics
  • Spinocerebellar Ataxias / genetics
  • Trinucleotide Repeat Expansion / genetics

Supplementary concepts

  • Lubs X-linked mental retardation syndrome