Hereditary spastic paraplegia type 69 (SPG69)
Evidence-based neurology checklist on hereditary spastic paraplegia type 69 (spg69): Genetics This is caused by mutations in the RAB3GAP2 gene on chromosome 1q The transmission is autosomal recessive Related gene disorders Clinical features
Genetics
- This is caused by mutations in the RAB3GAP2 gene on chromosome 1q
- The transmission is autosomal recessive
Related gene disorders
Clinical features
References
Related checklists
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