Phenotype #0000292129

Individual ID 00399041
Associated disease NMD
Diagnosis/Initial neuromuscular disorder
Diagnosis/Definite BMD
Phenotype details muscle biopsy reduced dystrophin
Inheritance Familial, X-linked recessive
Age/Examination 00y ()
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-01-15 16:40:49 +01:00 (CET)
Date last edited 2022-01-15 17:02:19 +01:00 (CET)

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