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 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 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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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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Murine model of autosomal dominant retinitis pigmentosa generated by targeted deletion at codon 307 of the rds –peripherin gene

By Humphries M.M.  

Human Molecular Genetics, Vol. 11, Iss. 9, 2002-05 ,pp. : 1005-1016

Oxford University Press

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