Oskar Schnappauf PhD , Hongying Wang PhD , Ivona Aksentijevich MD , Daniel L. Kastner MD, PhD , Ronald M. Laxer MD
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引用次数: 0
Abstract
The critical need for awareness and genetic testing of the SAMHD1 deletion in Ashkenazi Jewish patients is highlighted owing to its relatively high carrier frequency. Early detection can prevent severe disease complications through targeted therapy.
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