Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)

By Cremers F.P.M.  

Human Molecular Genetics, Vol. 10, Iss. 15, 2001-07 ,pp. : 1555-1562

Oxford University Press

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Mutations in HPRP3 , a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa

By Moore A.T.  

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

Oxford University Press

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Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31

By Deery E.C.  

Human Molecular Genetics, Vol. 11, Iss. 25, 2002-12 ,pp. : 3209-3219

Oxford University Press

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Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1

By Ars Elisabet   Serra Eduard   García Judit   Kruyer Helena   Gaona Antonia   Lázaro Conxi   Estivill Xavier  

Human Molecular Genetics, Vol. 9, Iss. 2, 2000-01 ,pp. : 237-247

Oxford University Press

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Nuclear bodies and compartmentalization of pre-mRNA splicing factors in higher plants

By Docquier Sarah   Tillemans Vinciane   Deltour Roger   Motte Patrick  

Chromosoma, Vol. 112, Iss. 5, 2004-02 ,pp. : 255-266

Springer Publishing Company

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