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. 2016 Feb 6;10(1-2):39–55. doi: 10.1080/19336918.2015.1093720

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© 2016 The Author(s). Published with license by Taylor & Francis Group, LLC

This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.

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Figure 6. — Identification of heterozygous carriers of syncytin-2 T522M (rs138651238) in normal pregnant women and severe pre-eclamptic (sPE) patients. (A) Frequency of T522M in normal pregnant women (n = 272) and sPE patients (n = 125). (B) Sequencing of syncytin-2 coding region revealed a C > T single-nucleotide polymorphism with amino acid substitution at 522 (T522M). MAF, minor allele frequency.