FTH1 ‐Related Neuroferritinopathy: A Rare Form of Neurodegeneration with Brain Iron Accumulation Mimicking Pontocerebellar Hypoplasia
Fields of Study & Subjects
Neurological diseases and metabolism
Metalloenzymes and iron-sulfur proteins
Metabolism and Genetic Disorders
Publication details
- Journal / source
- Movement Disorders Clinical Practice
- Publisher
- Wiley
- Volume
- 13
- Issue
- 5
- Pages
- 1333–1335
- Publication date
- 16 January 2026
- Language
- EN