Phenotypic and molecular characterization of a recurrent SPTAN1 mutation causing SPG91.
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| Title: | Phenotypic and molecular characterization of a recurrent SPTAN1 mutation causing SPG91. |
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| Authors: | Lan SC; School of Medicine, National Taiwan University College of Medicine, Taipei, Taiwan., Perng MD; Institute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.; School of Medicine, College of Life Sciences and Medicine, National Tsing Hua University, Hsinchu, Taiwan., Chang YY; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan., Chen YF; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan., Lan MY; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan. myl@ksts.seed.net.tw.; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan. myl@ksts.seed.net.tw.; Center for Mitochondrial Research and Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan. myl@ksts.seed.net.tw. |
| Source: | Molecular biology reports [Mol Biol Rep] 2025 May 21; Vol. 52 (1), pp. 476. Date of Electronic Publication: 2025 May 21. |
| Publication Type: | Journal Article; Case Reports |
| Journal Info: | Publisher: Reidel Country of Publication: Netherlands NLM ID: 0403234 Publication Model: Electronic Cited Medium: Internet ISSN: 1573-4978 (Electronic) Linking ISSN: 03014851 NLM ISO Abbreviation: Mol Biol Rep Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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