Phenotype #0000319046

Individual ID 00428109
Associated disease SCA
Phenotype details see paper; ..., abnormal eye movements, unable to perform tandem gait walking
Diagnosis/Initial spinocerebellar ataxia
Inheritance Familial, autosomal dominant
Diagnosis/Definite SCA27
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
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 2022-12-21 18:09:06 +01:00 (CET)
Date last edited 2022-12-21 19:29:58 +01:00 (CET)

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