Toure AISSATA, MD
Schwerpunktbereich
- Bewegungsstörungen
- Neurogenetik
- Genomik
- GP2 PhD
- Parkinson-Krankheit
- Genetische Ursachen der Parkinson-Erkrankung
- Ausbildungsangebote
- Ataxie
- Monogene Variante
- GWAS
Biographie
I have been working with the neurogenic laboratory since my internship in 2020 on inherited neurological condition including spinal muscular atrophy, ataxia, Huntington disease, Charcot Mari tooth, and Duchenne disease. I also perform DNA Extraction and DNA quantification. I’m currently working as a research assistant with a focus on the clinical and genetic feature of movement disorder.
