Hereditary spastic paraplegia type 89 (SPG89)
Evidence-based neurology checklist on hereditary spastic paraplegia type 89 (spg89): Genetics This is caused by mutations in the AMFR gene The gene is on chromosome 16 The transmission is autosomal recessive Neurological features Magnetic resonance imaging (MRI) brain
Genetics
- This is caused by mutations in the AMFR gene
- The gene is on chromosome 16
- The transmission is autosomal recessive
Neurological features
Magnetic resonance imaging (MRI) brain
References
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