Phenotype #0000154696

Individual ID 00206904
Associated disease AOA
Diagnosis/Initial ataxia-oculomotor apraxia
Diagnosis/Definite AOA-4
Phenotype details see paper; …
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen