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Case Reports

A case of spastic paraplegia-15 with a novel pathogenic variant in ZFYVE26 gene

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Pages 1198-1202 | Received 05 Mar 2019, Accepted 28 Jul 2019, Published online: 19 Aug 2019

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Grainne Mulkerrin, Marcondes C. França$suffix/text()$suffix/text(), Jasmin Lope, Ee Ling Tan & Peter Bede. (2022) Neuroimaging in hereditary spastic paraplegias: from qualitative cues to precision biomarkers. Expert Review of Molecular Diagnostics 22:7, pages 745-760.
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Articles from other publishers (4)

Ze-hua Lai, Xiao-ying Liu, Yuan-yue Song, Hai-yan Zhou & Li-li Zeng. (2023) Case report: Hereditary spastic paraplegia with a novel homozygous mutation in ZFYVE26. Frontiers in Neurology 14.
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Afshin Saffari, Melanie Kellner, Catherine Jordan, Helena Rosengarten, Alisa Mo, Bo Zhang, Oleksandr Strelko, Sonja Neuser, Marie Y Davis, Nobuaki Yoshikura, Naonobu Futamura, Tomoya Takeuchi, Shin Nabatame, Hiroyuki Ishiura, Shoji Tsuji, Huda Shujaa Aldeen, Elisa Cali, Clarissa Rocca, Henry Houlden, Stephanie Efthymiou, Birgit Assmann, Grace Yoon, Bianca A Trombetta, Pia Kivisäkk, Florian Eichler, Haitian Nan, Yoshihisa Takiyama, Alessandra Tessa, Filippo M Santorelli, Mustafa Sahin, Craig Blackstone, Edward Yang, Rebecca Schüle & Darius Ebrahimi-Fakhari. (2023) The clinical and molecular spectrum of ZFYVE26 -associated hereditary spastic paraplegia: SPG15 . Brain 146:5, pages 2003-2015.
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Arun Meyyazhagan & Antonio Orlacchio. (2022) Hereditary Spastic Paraplegia: An Update. International Journal of Molecular Sciences 23:3, pages 1697.
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Shao-Lun Hsu, Yi-Jiun Lu, Yu-Shuen Tsai, Hua-Chuan Chao, Jong-Ling Fuh, Yi-Chu Liao & Yi-Chung Lee. (2022) Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia. Journal of the Formosan Medical Association 121:1, pages 126-133.
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