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. 2023 Apr 14;5(1):vdad029. doi: 10.1093/noajnl/vdad029

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© The Author(s) 2023. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — (A) Family pedigrees of cases 1 and 2. Diagnosis and genetic analysis results are provided for the probands of each family. (B) Sanger sequencing results of all tumor and blood samples from cases 1 and 2 are shown via chromatograms using SnapGene software. PDGFRB c.2959C>T: p.R987W variant is confirmed in all samples.