The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding

By Young Philip J.  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2869-2877

Oxford University Press

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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

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A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophy

By Lefebvre S.   Burlet P.   Viollet L.   Bertrandy S.   Huber C.   Belser C.   Munnich A.  

Human Molecular Genetics, Vol. 11, Iss. 9, 2002-05 ,pp. : 1017-1027

Oxford University Press

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Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

By Kariya Shingo   Park Gyu-Hwan   Maeno-Hikichi Yuka   Leykekhman Olga   Lutz Cathleen   Arkovitz Marc S.   Landmesser Lynn T.   Monani Umrao R.  

Human Molecular Genetics, Vol. 17, Iss. 16, 2008-08 ,pp. : 2552-2569

Oxford University Press

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The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy

By Cartaud J.  

Human Molecular Genetics, Vol. 7, Iss. 12, 1998-11 ,pp. : 1927-1933

Oxford University Press

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