The role of the SMN gene in proximal spinal muscular atrophy

By Melki J.  

Human Molecular Genetics, Vol. 7, Iss. 10, 1998-10 ,pp. : 1531-1536

Oxford University Press

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A novel Caenorhabditis elegans allele, smn-1(cb131) , mimicking a mild form of spinal muscular atrophy, provides a convenient drug screening platform highlighting new and pre-approved compounds

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Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 245-260

Oxford University Press

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The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability

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Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2133-2143

Oxford University Press

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The human centromeric survival motor neuron gene ( SMN2 ) rescues embryonic lethality in Smn –/– mice and results in a mouse with spinal muscular atrophy

By Monani Umrao R.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 333-339

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Reduced survival motor neuron ( Smn ) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III

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Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 341-346

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