(Q32142955)
English
hereditary spastic paraplegia 38
hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15
- autosomal dominant spastic paraplegia 38
- autosomal dominant spastic paraplegia type 38
- SPG38
- hereditary spastic paraplegia type 38
- SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT
- SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38
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