Global Variome shared LOVD

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Phenotype #0000160451 Individual ID 00211970 Associated disease CNMX Phenotype details Severe Diagnosis/Initial myotubular myopathy Inheritance Familial Diagnosis/Definite CNMX Age/Examination - Age/Diagnosis - Age/Onset <1m Phenotype/Onset Severe neonatal weakness, global hypotonia and abolished tendon reflexes Protein - Owner name Jorge Oliveira Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2012-06-22 13:17:48 +02:00 (CEST) Date last edited 2012-06-22 15:49:43 +02:00 (CEST)

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