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By Moore A.T.  

Human Molecular Genetics, Vol. 11, Iss. 1, 2002-01 ,pp. : 87-92

Oxford University Press

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Positional Cloning of the Gene for X-Linked Retinitis Pigmentosa 3: Homology with the Guanine-Nucleotide-Exchange Factor RCC1

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Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1035-1041

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Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy

By Bühler Dirk   Raker Veronica   Lührmann Reinhard   Fischer Utz  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2351-2357

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Identification and Characterization of Human Genes Encoding Hprp3p and Hprp4p, Interacting Components of the Spliceosome

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Human Molecular Genetics, Vol. 6, Iss. 12, 1997-11 ,pp. : 2117-2126

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Systemic splicing factor deficiency causes tissue-specific defects: a zebrafish model for retinitis pigmentosa

By Linder Bastian   Dill Holger   Hirmer Anja   Brocher Jan   Lee Gek Ping   Mathavan Sinnakaruppan   Bolz Hanno Jrn   Winkler Christoph   Laggerbauer Bernhard   Fischer Utz  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 368-377

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