Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

By Bowne S.J.  

Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 559-568

Oxford University Press

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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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A Ninth Locus ( RP18 ) for Autosomal Dominant Retinitis Pigmentosa Maps in the Pericentromeric Region of Chromosome 1

By Ying Xu Su   Schwartz Marianne   Rosenberg Thomas   Gal Andreas  

Human Molecular Genetics, Vol. 5, Iss. 8, 1996-01 ,pp. : 1193-1197

Oxford University Press

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Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10)

By Tam Lawrence C.S.   Kiang Anna-Sophia   Kennan Avril   Kenna Paul F.   Chadderton Naomi   Ader Marius   Palfi Arpad   Aherne Aileen   Ayuso Carmen   Campbell Matthew   Reynolds Alison   McKee Alex   Humphries Marian M.   Farrar G. Jane   Humphries Pete  

Human Molecular Genetics, Vol. 17, Iss. 14, 2008-07 ,pp. : 2084-2100

Oxford University Press

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Distinct gene expression profiles and reduced JNK signaling in retinitis pigmentosa caused by RP1 mutations

By Liu Jiewu  

Human Molecular Genetics, Vol. 14, Iss. 19, 2005-10 ,pp. : 2945-2958

Oxford University Press

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