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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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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A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotype

By Gladman Jordan T.   Bebee Thomas W.   Edwards Chris   Wang Xueyong   Sahenk Zarife   Rich Mark M.   Chandler Dawn S.  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4239-4252

Oxford University Press

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A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2

By Monani Umrao R.  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1177-1183

Oxford University Press

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Regulation of murine survival motor neuron ( Smn ) protein levels by modifying Smn exon 7 splicing

By DiDonato C.J.  

Human Molecular Genetics, Vol. 10, Iss. 23, 2001-11 ,pp. : 2727-2736

Oxford University Press

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