Ataxia with oculomotor apraxia type 1 associated with mutation in the APTX gene: A case study and literature review
R Albaradie, A Alharbi, G Alsaffar… - Experimental and …, 2022 - spandidos-publications.com
Cerebellar ataxia is a disorder characterized by a broad spectrum of phenotypes. Ataxia with
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …
oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease presenting with early …