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Jun 6, 2019 (publication date) through Jul 21, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Xiao XW, Du J, Jiao B, Liao XX, Zhou L, Liu XX, Yuan ZH, Guo LN, Wang X, Shen L, Lin ZY. Novel ATL1 mutation in a Chinese family with hereditary spastic paraplegia: A case report and review of literature. World J Clin Cases 2019; 7(11): 1358-1366 [PMID: 31236401 DOI: 10.12998/wjcc.v7.i11.1358] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v7/i11/1358.htm |
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| 1 |
Carolyn M. Kelly, Peter J. Zeiger, Vinodh Narayanan, Keri Ramsey, Holger Sondermann. A novel insertion mutation in atlastin 1 is associated with spastic quadriplegia, increased membrane tethering, and aberrant conformational switching. Journal of Biological Chemistry 2022; 298(1): 101438 doi: 10.1016/j.jbc.2021.101438
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Salimata Diarra, Thomas Coulibaly, Kékouta Dembélé, Nyater Ngouth, Lassana Cissé, Seybou H. Diallo, Madani Ouologuem, Salimata Diallo, Oumar Coulibaly, Koumba Bagayoko, Dramane Coulibaly, Assiatou Simaga, Hammadoun A. Sango, Mahamadou Traoré, Steve Jacobson, Kenneth H. Fischbeck, Guida Landouré, Cheick O. Guinto. Hereditary spastic paraplegia in Mali: epidemiological and clinical features. Acta Neurologica Belgica 2023; 123(6): 2155 doi: 10.1007/s13760-022-02113-w
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Kaalindi Misra, Milena Ślęczkowska, Silvia Santoro, Monique M. Gerrits, Elisabetta Mascia, Margherita Marchi, Erika Salvi, Hubert J. M. Smeets, Janneke G. J. Hoeijmakers, Filippo Giovanni Martinelli Boneschi, Massimo Filippi, Giuseppe Lauria Pinter, Catharina G. Faber, Federica Esposito. Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases. International Journal of Molecular Sciences 2024; 25(13): 7248 doi: 10.3390/ijms25137248
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