(Q32142811)
English
hereditary spastic paraplegia 29
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1.
- SPG29
- autosomal dominant spastic paraplegia 29
- Autosomal dominant spastic paraplegia type 29
- SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT
- SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT; SPG29
- hereditary spastic paraplegia type 29
Statements
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