Global Variome shared LOVD

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Phenotype #0000285078 Individual ID 00391755 Associated disease MRX1 Phenotype details Myoclonus, Absent speech, Atypical absence seizure, Multifocal epileptiform discharges, Severe global developmental delay Diagnosis/Initial - Inheritance Familial, X-linked dominant Diagnosis/Definite - Age/Examination 05y (5 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Birth_Details - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2021-11-18 14:35:18 +01:00 (CET) Date last edited 2021-11-18 14:57:09 +01:00 (CET)

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