Global Variome shared LOVD

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Phenotype #0000236668 Individual ID 00311420 Associated disease NEBDM Diagnosis/Initial distal myopathy Diagnosis/Definite - Phenotype details see paper; ..., congenital asymmetric distal myopathy with hemifacial weakness Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Vilma-Lotta Lehtokari Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Vilma-Lotta Lehtokari Date created 2020-09-25 10:27:31 +02:00 (CEST) Date last edited 2022-10-04 19:41:47 +02:00 (CEST)

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