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. 2015 Oct 26;16:98. doi: 10.1186/s12881-015-0245-3

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© Miyazaki et al. 2015

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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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Fig. 2 — Pathogenic nucleotide alteration of the PKHD1 gene identified in the paternal allele. Sample names are indicated on the left: FHU14–046 (I-1, father), FHU13–047 (I-2, mother), FHU13–049 (II-1, healthy sibling), FHU13–051 (II-3, proband), and FHU13–068 (II-5, amniotic fluid)