Ataxia with Oculomotor Apraxia Type 1—New Mutation, Characteristic Phenotype
Sign Up to like & getrecommendations! Published in 2019 at "Movement Disorders Clinical Practice"
DOI: 10.1002/mdc3.12725
Abstract: A 22-year-old man is the third of four siblings from a family with a high degree of consanguinity. At 18 months, he was first noted to be unsteady and subsequently developed a slurred speech. His… read more here.
Keywords: head; apraxia type; ataxia oculomotor; oculomotor apraxia ... See more keywords