Localisation of a Gene for Central Areolar Choroidal Dystrophy to Chromosome 17p

By Lotery Andrew J.   Ennis Kevin T.   Silvestri Giuliana   Nicholl Suzanne   McGibbon David   Collins Alan D.   Hughes Anne E.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 705-708

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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A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1

By Payne A.M.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 273-277

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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Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone–rod dystrophy

By Wilkie Susan E.   Newbold RichardJ.  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3065-3073

Oxford University Press

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