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Article

Localisation of a gene for central areolar choroidal dystrophy to chromosome 17p

1 May 1996

Abstract excerpt

Central areolar choroidal dystrophy (CACD) is a rare inherited retinal disease which causes progressive profound loss of vision in patients during their 4th decade. We have identified a Northern Irish family with 19 affected individuals in three living generations. We have performed a total genome search and established linkage of CACD in this family to chromosome 17p (multipoint Zmax = 5.65 at D17S938). The...

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PMID: 8733141
DOI: 10.1093/hmg/5.5.705

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