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"Ataxia," "early-onset," with oculomotor apraxia hypoalbuminemia
- ... with oculomotor apraxia type 3 Genetic Testing Registry: Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Genetic Testing Registry: Spinocerebellar ataxia, autosomal recessive, with ...
- ... causing the characteristic movement problems of ataxia with oculomotor apraxia type 1. More About This Health Condition AOA AOA1 APTX_HUMAN ataxia 1, early onset with hypoalbuminemia AXA1 EAOH EOAHA FHA-HIT Tests of APTX ...