Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa

By Bowne Sara J.   Daiger Stephen P.   Hims Matthew M.  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2121-2128

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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Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho –/– mice

By Ayuso C.  

Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 547-558

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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