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

Oxford University Press

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Characterization of Survival Motor Neuron (SMN T ) Gene Deletions in Asymptomatic Carriers of Spinal Muscular Atrophy

By Wang Ching H.   Xu Jin   Carter Todd A.   Ross Barbara M.   Dominski Mary K.   Bellcross Cecelia A.   Penchaszadeh Graciela K.   Munsat Theodore L.   Conrad Gilliam T.  

Human Molecular Genetics, Vol. 5, Iss. 3, 1996-01 ,pp. : 359-365

Oxford University Press

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SMNΔ7, the major product of the centromeric survival motor neuron ( SMN2 ) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN

By Le Thanh T.  

Human Molecular Genetics, Vol. 14, Iss. 6, 2005-03 ,pp. : 845-857

Oxford University Press

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The Survival Motor Neuron Protein in Spinal Muscular Atrophy

By Coovert Daniel D.  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1205-1214

Oxford University Press

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Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy

By Jablonka S.  

Human Molecular Genetics, Vol. 10, Iss. 5, 2001-03 ,pp. : 497-505

Oxford University Press

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