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1. Coexistence of Atrioventricular Nodal Reentrant Tachycardia and Idiopathic Left Ventricular Outflow-Tract Tachycardia

2. Multiple Arrhythmogenic Substrate for Tachycardia in a Patient with Frequent Palpitations

7. Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities

8. Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder

12. Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder

15. Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1

17. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

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