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. 2024 May 23;15:1380552. doi: 10.3389/fgene.2024.1380552

FIGURE 2.

FIGURE 2

Diagnostic Timeline. At 15, the patient underwent genetic tests for neurodevelopmental symptoms without diagnostic yield. Referral to the PCPM clinic led to Whole Exome Sequencing (WES), unveiling a pathogenic HNRNPU mutation. WES data informed two subsequent genetic inquiries. Created with BioRender.com.