(Q32143018)
English
hereditary spastic paraplegia 42
A hereditary spastic paraplegia that has material basis in mutation in the SLC33A1 gene on chromosome 3q25.31.
- autosomal dominant spastic paraplegia 42
- autosomal dominant spastic paraplegia type 42
- SPG42
- SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42
- hereditary spastic paraplegia type 42
- SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT
Statements
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Identifiers
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