The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy

By Newbold R.J.  

Human Molecular Genetics, Vol. 10, Iss. 1, 2001-01 ,pp. : 47-54

Oxford University Press

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Functional analysis of cone–rod homeobox (CRX) mutations associated with retinal dystrophy

By Chen S.  

Human Molecular Genetics, Vol. 11, Iss. 8, 2002-04 ,pp. : 873-884

Oxford University Press

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Mutations in the retinal guanylate cyclase ( RETGC-1 ) gene in dominant cone–rod dystrophy

By Hunt D.M.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1179-1184

Oxford University Press

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Autosomal recessive retinitis pigmentosa and cone–rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

By Blankenagel A.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 355-362

Oxford University Press

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Localisation of a Gene for Dominant Cone-Rod Dystrophy ( CORD6 ) to Chromosome 17p

By Kelsell Rosemary E.   Evans Kevin   Gregory Cheryl Y.   Moore Anthony T.   Bird Alan C.   Hunt David M.  

Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 597-600

Oxford University Press

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