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- W2891933712 abstract "Following detection of a homozygous variant in the ribonuclease H2 Subunit B (RNASEH2B; NM_024570.3) gene in a patient with sporadic, pure hereditary spastic paraplegia (HSP), we reviewed the literature to find only four published cases (three by Crow[1] and one by Travaglini).[2]" @default.
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- W2891933712 date "2018-09-17" @default.
- W2891933712 modified "2023-09-25" @default.
- W2891933712 title "RNASEH2B Pathogenic Gene Variant in Uncomplicated Hereditary Spastic Paraplegia: Report of a New Patient" @default.
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- W2891933712 doi "https://doi.org/10.1055/s-0038-1672174" @default.
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