(Q32142548)
English
hereditary spastic paraplegia 10
hereditary spastic paraplegia that has material basis in mutation in the KIF5A gene on chromosome 12q13
- autosomal dominant spastic paraplegia 10
- autosomal dominant spastic paraplegia type 10
- SPG10
- hereditary spastic paraplegia type 10
- SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT
- Spastic Paraplegia 10 With or Without Peripheral Neuropathy
- SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10
Statements
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C192058
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Identifiers
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