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. 2014 May 8;4(2):15. doi: 10.7603/s40681-014-0015-0

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© China Medical University 2014

Open Access This article is distributed under terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided original author(s) and source are credited.

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Fig. 1 — (A) Pedigree of PKC/PKD Taiwanese family: persons designated by sex, disease status (filled symbols represent patients, open symbols normal persons). Index case indicated by arrow. (B) Sequencing results of mutation in PRRT2 gene of index case. Arrow indicates one-base C inserted at nucleotide 650 (c.650insC), causing protein translation shift and stopping after seventh residue.

Fig. 1 — (A) Pedigree of PKC/PKD Taiwanese family: persons designated by sex, disease status (filled symbols represent patients, open symbols normal persons). Index case indicated by arrow. (B) Sequencing results of mutation in PRRT2 gene of index case. Arrow indicates one-base C inserted at nucleotide 650 (c.650insC), causing protein translation shift and stopping after seventh residue.