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De novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing

Step 6: Inspect the solution Hold the vial up to a light source and examine the solution carefully

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Notably, high-quality clinical evidence directly targeting DGE is scarce, with most studies conducted in models of chronic constipation, gastrointestinal motility disorders, or irritable bowel syndrome (IBS)