Global Variome shared LOVD

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Phenotype #0000084263 Individual ID 00106459 Associated disease MYOP Phenotype details congenital myopathy with fibre type disproportion, normal CK values; CPK: normal Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset <0d Phenotype/Onset - Protein - Owner name Wolfram Kress Database submission license No license selected Created by Wolfram Kress Date created 2012-08-03 11:26:45 +02:00 (CEST) Date last edited N/A

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