Transient neonatal multiple acyl-CoA dehydrogenase deficiency
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Zentrum für Stoffwechselerkrankungen (Villa Metabolica) der Universitätsmedizin Mainz
Zentrum für Seltene Erkrankungen Mainz Universitätsmedizin Mainz
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Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
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                    80336 München
                
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- Beta-propeller protein-associated neurodegeneration
- Neuroferritinopathy
- Neurodegeneration with brain iron accumulation
- Pantothenate kinase-associated neurodegeneration
- Rare ataxia
- Huntington disease
- Leukodystrophy
- COASY protein-associated neurodegeneration
- Hereditary spastic paraplegia
- Myasthenia gravis
- Infantile neuroaxonal dystrophy
- Mitochondrial membrane protein-associated neurodegeneration
- Atypical pantothenate kinase-associated neurodegeneration
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease