Mutation in the splicing factor Hprp3p linked to retinitis pigmentosa impairs interactions within the U4/U6 snRNP complex

By Gonzalez-Santos Juana Maria   Cao Huibi   Duan Rongqi Cathleen   Hu Jim  

Human Molecular Genetics, Vol. 17, Iss. 2, 2008-01 ,pp. : 225-239

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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Characterization of a gene encoding Survival Motor Neuron (SMN)-related protein, a constituent of the spliceosome complex

By Ponting C.P.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2149-2156

Oxford University Press

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Molecular characterization and expression of p63 isoforms in human keloids

By Felice B.   Wilson R.   Nacca M.   Ciarmiello L.   Pinelli C.  

Molecular Genetics and Genomics, Vol. 272, Iss. 1, 2004-08 ,pp. : 28-34

Springer Publishing Company

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Characterization of genes encoding translation initiation factor eIF-2 in mouse and human: sex chromosome localization, escape from X-inactivation and evolution

By Affara N.A.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1725-1737

Oxford University Press

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