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- W59631644 abstract "In this case-report we present a patient with a genetic disease which was first diagnosed in his eighties. The genetic disease is a rare neurologic disease, Kennedy's disease or spinobulbar muscular atrophy (SBMA). We also discuss the genetics of the disease and developments of future therapies." @default.
- W59631644 created "2016-06-24" @default.
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- W59631644 date "2010-02-01" @default.
- W59631644 modified "2023-09-23" @default.
- W59631644 title "Op onduidelijke wijze in een rolstoel beland" @default.
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- W59631644 doi "https://doi.org/10.1007/bf03096177" @default.
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