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. 2014 Apr 16;1:4. doi: 10.1186/2052-6687-1-4

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© Downs et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fine mapping using haplotype analysis. SNP genotypes for 10 PRA cases and 16 PRA controls, over the 668 kb “Affected haplotype” identified during the GWA study. Inferred phasing of the 21 SNP markers revealed six unique haplotypes. Haplotype number 1 (yellow) is homozygous in 8/10 cases, but none of the controls.