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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hnRNP A1 functions with specificity in repression of SMN2 exon 7 splicing

By Kashima Tsuyoshi   Rao Nishta   David Charles J.   Manley James L.  

Human Molecular Genetics, Vol. 16, Iss. 24, 2007-12 ,pp. : 3149-3159

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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An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN

By Lorson Christian L.   Androphy Elliot J.  

Human Molecular Genetics, Vol. 9, Iss. 2, 2000-01 ,pp. : 259-265

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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