Pharming Group Spotlights New Insights Into APDS Diagnosis With Webcast On Cell-Published Study Linking Genetic Variants To PI3Kδ Hyperactivity In Over 100 Cases

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Researchers identified variants which may cause activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS)
Results enable clinical genetic testing labs to appropriately reclassify VUSs, accelerating the path to a definitive APDS diagnosis for many patients
Findings reveal APDS may be more prevalent than previously estimated

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