Hereditary spastic paraplegia type 61 (SPG61)
Evidence-based neurology checklist on hereditary spastic paraplegia type 61 (spg61): Genetics This is caused by mutations in the ARL61P1 gene on chromosome 16p The transmission is autosomal recessive The onset age is 14 months Clinical features
Genetics
- This is caused by mutations in the ARL61P1 gene on chromosome 16p
- The transmission is autosomal recessive
- The onset age is 14 months
Clinical features
References
Related checklists
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