Hereditary spastic paraplegia type 37 (SPG37)
Evidence-based neurology checklist on hereditary spastic paraplegia type 37 (spg37): Genetics This is caused by mutations in chromosome 8p The transmission is autosomal dominant Clinical features Magnetic resonance imaging (MRI) brain
Genetics
- This is caused by mutations in chromosome 8p
- The transmission is autosomal dominant
Clinical features
Magnetic resonance imaging (MRI) brain
References
Related checklists
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