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An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1)

Sauer, C. G. ; Schworm, H. D. ; Ulbig, M. ; Blankenagel, A. ; Rohrschneider, K. ; Pauleikhoff, D. ; Grimm, T. ; Weber, Bernhard H. F.



Abstract

Autosomal dominant North Carolina macular dystrophy (NCMD) or central areolar pigment epithelial dystrophy (CAPED) is an allelic disorder that maps to an approximately 7.2 cM interval between DNA markers at D6S424 and D6S1671 on 6q14-q16.2. The further refinement of the disease locus has been hindered by the lack of additional recombination events involving the critical region. In this study, we ...

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