Global Variome shared LOVD

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Phenotype #0000159929 Individual ID 00211447 Associated disease MFM Phenotype details progressive weakness (distal > proximal), distal sensory deficits,perivascular mononuclear cellsepineurium; peripheral neuropathy; no cardiac involvement; EMG severe polyradiculoneuropathy, neurogenic MUPs, fibrillation potentials; Diagnosis/Initial myofibrillar myopathy Inheritance Isolated (sporadic) Diagnosis/Definite MFM Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2010-01-24 15:43:12 +01:00 (CET) Date last edited 2012-03-09 19:08:25 +01:00 (CET)

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