Hereditary spastic paraplegia type 32 (SPG32)
Evidence-based neurology checklist on hereditary spastic paraplegia type 32 (spg32): Genetics This is caused by mutations in chromosome 14q The transmission is autosomal recessive Clinical features Magnetic resonance imaging (MRI) brain: features
Genetics
- This is caused by mutations in chromosome 14q
- The transmission is autosomal recessive
Clinical features
Magnetic resonance imaging (MRI) brain: features
References
Related checklists
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