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Spectrum of SPG4 Mutations in a Large Collection of North American Families With Hereditary Spastic Paraplegia

机译：SPG4突变在北美家庭的大集合中的SPG4突变，具有遗传性痉挛性截瘫患者

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Inge A. Meijer; Collette K. Hand; P. Cossette; Denise A. Figlewicz; Guy A. Rouleau;
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年度 2002
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1. Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia. [J] . Erichsen AK, Inderhaug E, Mattingsdal M, European journal of neurology: the official journal of the European Federation of Neurological Societies . 2007,第7期

机译：一组患有SPG4遗传性痉挛性截瘫的挪威患者中的七个新突变和四个外显子缺失。
2. Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia [J] . V. A. Kadnikova, G. E. Rudenskaya, A. A. Stepanova, Scientific reports. . 2019,第1期

机译：俄罗斯痉挛性痉挛性截瘫患者的副盐（SPG4）和ATL1（SPG3A）基因的突变谱
3. Mutational spectrum of the SPG4 ( SPAST ) and SPG3A ( ATL1 ) genes in Spanish patients with hereditary spastic paraplegia [J] . Victoria álvarez, Elena Sánchez-Ferrero, Christian Beetz, BMC Neurology . 2010,第1期

机译：SPG4（SPAST）和SPG3A（ATL1）基因的突变谱在西班牙痉挛性痉挛性截瘫患者中
4. Analysis of Test-Retest Repeatability of Gait Analysis Parameters in Hereditary Spastic Paraplegia [C] . Armando Coccia, Federica Amitrano, Pietro Balbi, IEEE International Symposium on Medical Measurements and Applications . 2021

机译：遗传痉挛性截瘫术中的步态分析参数的试验 - 重复性分析
5. Development and Manipulation of a Drosophila Model for Toxic Effects of Mutated M1 Spastin in Hereditary Spastic Paraplegia Treatment [D] . Yiantsos, Ioanna. 2019

机译：果蝇突变M1 Spastin在遗传性痉挛性截瘫治疗中毒性作用的果蝇模型的开发和操纵。
6. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia [O] . Victoria Álvarez, Elena Sánchez-Ferrero, Christian Beetz, 2010

机译：西班牙遗传性痉挛性截瘫患者中SPG4（SPAST）和SPG3A（ATL1）基因的突变谱
7. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia [O] . Victoria Álvarez, null null, Elena Sánchez-Ferrero, 2016

机译：西班牙遗传性痉挛性截瘫患者中SPG4（SPAST）和SPG3A（ATL1）基因的突变谱

Spectrum of SPG4 Mutations in a Large Collection of North American Families With Hereditary Spastic Paraplegia

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