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Table S1. Clinical details of the 13 PGLs included in the study, with their KMT2D expressional results from qRT-PCR, copy number and immunohistochemical analyses. Table S2. Summary of the 13 non-synonymous exclusively somatic mutations identified in 3 PGLs via whole-exome sequencing. The previously known constitutional SDHB mutation of case 3 is not shown. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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Stenman et al. (2015) studied this question.
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