Phenotype #0000130185

Individual ID 00000269
Associated disease MC3DN
Diagnosis/Initial mitochondrial complex III deficiency
Diagnosis/Definite MC3DN-5
Phenotype details see paper; ...
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
Date created 2018-07-09 13:41:19 +02:00 (CEST)
Date last edited N/A

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