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. 2014 Jun 26;9(6):e100560. doi: 10.1371/journal.pone.0100560

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© 2014 Alcalde et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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ARVC clinically affected individuals (grey round/square) and genetic carriers (black point inside round/square), not evaluated (question mark inside round/square), death (round/square with slash) and sudden death (grey round/square with slash). A- Family A. Index case is III.4 and carries c.2203 C>G (p.R735*) in PKP2 . B- Family B. Index case is III.2 and carries c.2013delC (p.P671Pfs12*) in PKP2. C- Family C. Index case is II.4 and carries c.1912C>T (p.Q638*) in PKP2. D- Family D. Index case is II.1 and carries c.1237C> T (p.R413*). E- Family E. Index case is III.2, who carries a homozygous c.2440T>C (p.C814R) variation in the DSG2 gene.