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Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan.

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作者： Briese M ^[1] ; Esmaeili B ; Fraboulet S ; Burt EC ; Christodoulou S ; Towers PR ; Davies KE ; Sattelle DB

作者单位： MRC Functional Genomics Unit, Department of Physiology Anatomy and Genetics, University of Oxford, South Parks Road, Oxford OX1 3QX, UK. ^[1]

关键词 Animals Caenorhabditis elegans Caenorhabditis elegans Proteins Disease Models Animal 动物新小杆线虫漂亮疾病模型基因缺失长寿运动活动肌萎缩脊髓性

发布时间 2013-11-20

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Human Molecular Genetics

2009年18卷1期

97-104页

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Human Molecular Genetics

2009年18卷1期

97-104页

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Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan.

Human Molecular Genetics

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Human Molecular Genetics

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Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan.

Human Molecular Genetics

相似文献

Human Molecular Genetics

相关期刊

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