All individuals with variants in gene SPG21

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00473355 Fam206276Pat621 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - paraplegia onset 7y, spastic gait, frequent falling, increased DTR, spastic paraplegia, frontotemporal mild cortical atrophy, diffuse cerebellar atrophy and thinning of corpus callosum reported in brain MRI 1 1 Johan den Dunnen
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