Oguchi disease: suggestion of linkage to markers on chromosome 2q.

Author:

Maw M A,John S,Jablonka S,Muller B,Kumaramanickavel G,Oehlmann R,Denton M J,Gal A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. In the present study markers which map to distal chromosome 2q were typed in an inbred Oguchi pedigree. The segregation data obtained suggested that the affected subjects are homozygous by descent for a region between D2S172 and D2S345. An intragenic SAG polymorphism was homozygous in all affected people and a recombination event suggested that SAG maps proximal to D2S345. Collectively, these findings support the hypothesis that a defect in S antigen may be responsible for Oguchi disease,1995

2. La Maladie d'Oguchi;Francois, J.; Verriest, G.; De Rouck, A.;Ophthalmologica,1956

3. Oguchi's disease;Carr, R.E.; Gouras, P.;Arch Ophthalnmol,1965

4. The influence of arrestin (48K protein) and rhodopsin kinase on visual transduction;Palczewski, K.; Rispoli, G.; Detwiler, P.B.;Neuron,1992

5. Regulation of rhodopsin dephosphorylation by arrestin;Palczewski, K.; McDowell, J.H.; Takes, S.; Ingebritsen, T.S.; Hargrave, P.A.;_7 Biol Chem,1989

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