| Original language | English |
|---|---|
| Pages (from-to) | 2125-2126 |
| Number of pages | 2 |
| Journal | Movement Disorders |
| Volume | 39 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - Nov 2024 |
| Externally published | Yes |
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 journal › Letter › peer-review
1
Citation
(Scopus)