Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses (vol 59, pg 163, 2014)

Ishiura Hiroyuki; Takahashi Yuji; Hayashi Toshihiro; Saito Kayoko; Furuya Hirokazu; Watanabe Mitsunori; Murata Miho; Suzuki Mikiya; Sugiura Akira; Sawai Setsu; Shibuya Kazumoto; Ueda Naohisa; Ichikawa Yaeko; Kanazawa Ichiro; Goto Jun; Tsuji Shoji

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Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses (vol 59, pg 163, 2014)

机译：基于综合突变分析的日本人群遗传性痉挛性截瘫的分子流行病学和临床范围（第59卷，第163页，2014年）

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来源
《Journal of human genetics》 |2016年第4期|共2页
作者
Ishiura Hiroyuki; Takahashi Yuji; Hayashi Toshihiro; Saito Kayoko; Furuya Hirokazu; Watanabe Mitsunori; Murata Miho; Suzuki Mikiya; Sugiura Akira; Sawai Setsu; Shibuya Kazumoto; Ueda Naohisa; Ichikawa Yaeko; Kanazawa Ichiro; Goto Jun; Tsuji Shoji;
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正文语种 eng
中图分类医学遗传学;
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1. Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses (vol 59, pg 163, 2014) [J] . Ishiura Hiroyuki, Takahashi Yuji, Hayashi Toshihiro, Journal of human genetics . 2016,第4期

机译：基于综合突变分析的日本人群遗传性痉挛性截瘫的分子流行病学和临床范围（第59卷，第163页，2014年）
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. Expanding the Clinical Spectrum of SPG11 Gene Mutations in Recessive Hereditary Spastic Paraplegia with Thin Corpus Callosum [O] . Alice Abdel Aleem, Nourhan Abu-Shahba, Dominika Swistun, -1

机译：用薄胼callosum扩展隐性遗传性痉挛性截瘫患者的SPG11基因突变的临床谱
5. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum [O] . Alice Abdel Aleem, Nourhan Abu-Shahba, Dominika Swistun, 2011

机译：用薄胼callosum扩展隐性遗传性痉挛性截瘫患者的SPG11基因突变的临床谱

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses (vol 59, pg 163, 2014)

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