Global Variome shared LOVD

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Phenotype #0000347953 Individual ID 00460225 Associated disease MDC Phenotype details see paper; ..., motor retardation; mild hypertonia; EEG normal; MR cerebellar hypoplasia, mild development delay Diagnosis/Initial congenital muscular dystrophy/myopathy Diagnosis/Definite MMYAT Inheritance Familial, autosomal recessive Age/Examination 3y (3 years) Age/Diagnosis - 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 2025-01-21 21:16:51 +01:00 (CET) Date last edited N/A

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