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Response to Mortimer et al. “Clinical and molecular profiling in GNAO1 permits phenotype–genotype correlation”

  • Amaia Lasa-Aranzasti
  • , Gonzalo P. Solis
  • , Vladimir L. Katanaev
  • , Belén Pérez-Dueñas*
  • *Corresponding author for this work
  • University Hospital Vall d'Hebron
  • Autonomous University of Barcelona
  • European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA
  • University of Geneva
  • Far Eastern Federal University
  • European Reference Network-Rare Neurological Diseases (ERN-RND)
  • Centro de Investigación en Red de Enfermedades Raras (CIBERER)

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)2125-2126
Number of pages2
JournalMovement Disorders
Volume39
Issue number11
DOIs
Publication statusPublished - Nov 2024
Externally publishedYes

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