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For: Elsayed LEO, Eltazi IZ, Ahmed AE, Stevanin G. Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview. Front Mol Biosci 2021;8:690899. [PMID: 34901147 DOI: 10.3389/fmolb.2021.690899] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 13.0] [Reference Citation Analysis]
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6 Costa AC, Sousa MM. The Role of Spastin in Axon Biology. Front Cell Dev Biol 2022;10:934522. [DOI: 10.3389/fcell.2022.934522] [Reference Citation Analysis]
7 Parodi L, Pujol C. Hereditary spastic paraplegia type 56: what a mouse can tell – a narrative review. Journal of Bio-X Research 2022;5:55-63. [DOI: 10.1097/jbr.0000000000000127] [Reference Citation Analysis]
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9 Ung DC, Tricoire L, Pietrancosta N, Zlatanovic A, Pode-shakked B, Raas-rothschild A, Elpeleg O, Abu-libdeh B, Hamed N, Papon M, Marouillat S, Thépault R, Stevanin G, Lambolez B, Toutain A, Hepp R, Laumonnier F. GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses.. [DOI: 10.1101/2022.05.16.22274994] [Reference Citation Analysis]
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11 Chouery E, Mehawej C, Megarbane A. A novel homozygous variant in RNF170 causes hereditary spastic paraplegia: a case report and review of the literature. Neurogenetics 2022;23:85-90. [DOI: 10.1007/s10048-022-00685-6] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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13 Mahungu AC, Monnakgotla N, Nel M, Heckmann JM. A review of the genetic spectrum of hereditary spastic paraplegias, inherited neuropathies and spinal muscular atrophies in Africans. Orphanet J Rare Dis 2022;17:133. [PMID: 35331287 DOI: 10.1186/s13023-022-02280-2] [Reference Citation Analysis]