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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An 11 Base Pair Duplication in Exon 6 of the SMN Gene Produces a Type I Spinal Muscular Atrophy (SMA) Phenotype: Further Evidence For SMN as the Primary SMA-Determining Gene

By Parsons D. Williams   McAndrew Patricia E.   Monani Umrao R.   Mendell Jerry R.   Burghes Arthur H. M.   Prior Thomas W.  

Human Molecular Genetics, Vol. 5, Iss. 11, 1996-11 ,pp. : 1727-1732

Oxford University Press

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Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?

By Ohndorf U-M.   Steegborn C.   Rossoll W.   Kröning A-K.   Jablonka S.   Sendtner M.  

Human Molecular Genetics, Vol. 11, Iss. 1, 2002-01 ,pp. : 93-105

Oxford University Press

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A feedback loop regulates splicing of the spinal muscular atrophy-modifying gene, SMN2

By Jodelka Francine M.   Ebert Allison D.   Duelli Dominik M.   Hastings Michelle L.  

Human Molecular Genetics, Vol. 19, Iss. 24, 2010-12 ,pp. : 4906-4917

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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