Combined oxidative phosphorylation defect type 13
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Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
Friedrich-Baur-Institut am Klinikum der Ludwig-Maximilians-Universität München
LMU Klinikum München
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80336 München
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- Infantile neuroaxonal dystrophy
- Hereditary spastic paraplegia
- Huntington disease
- Atypical pantothenate kinase-associated neurodegeneration
- Pantothenate kinase-associated neurodegeneration
- Neuroferritinopathy
- Mitochondrial membrane protein-associated neurodegeneration
- Neurodegeneration with brain iron accumulation
- Classic pantothenate kinase-associated neurodegeneration
- Mitochondrial disease
- Beta-propeller protein-associated neurodegeneration
- Leukodystrophy
- COASY protein-associated neurodegeneration
- Rare ataxia