Hereditary spastic paraplegia type 36 (SPG36)
Evidence-based neurology checklist on hereditary spastic paraplegia type 36 (spg36): Genetics This is caused by mutations in chromosome 12q The transmission is autosomal dominant The mean onset age is 24 years Clinical features Magnetic resonance imaging (MRI) brain
Genetics
- This is caused by mutations in chromosome 12q
- The transmission is autosomal dominant
- The mean onset age is 24 years
Clinical features
Magnetic resonance imaging (MRI) brain
References
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