All individuals with variants in gene GBA2

5 entries on 1 page. Showing entries 1 - 5.
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AscendingIndividual ID     

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00054872 Pat15 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG46 hereditary spastic paraplegia, ataxia, cataract, neuropathy, mild ID, thin corpus callosum, white matter changes 1 1 Erik-Jan Kamsteeg
00294856 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00294857 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 66 Mohammed Faruq
00299449 - family, 2 affected HSP46 F - Ethiopia African - - - - SPG46 Dementia Ataxia Dystonia 2 2 Katja Kloth
00473359 Fam206565Pat628 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - paraplegia muscle weakness and atrophy, bulbar dysfunction, dysarthria, spastic gait, pes cavus, cerebellar sign, increased DTR, chronic L5-S1 motor neuropathy reported in EMG and normal brain MRI 1 1 Johan den Dunnen
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