Skip to main content
. Author manuscript; available in PMC: 2015 Sep 1.
Published in final edited form as: J Clin Neurosci. 2014 May 6;21(9):1627–1631. doi: 10.1016/j.jocn.2013.11.048

Fig. 1.

Fig. 1

Identification of ataxia with oculomotor apraxia type 2 in a South American woman. (A) Coronal (left), sagittal (middle) and axial (right) T1-weighted brain MRI of III.4 showing severe cerebellar (particularly vermal) atrophy. (B) Pedigree of the reported family. The proband patient III.4 carries both c.994 C>T and c.6848delCAGA mutations. II.7 is a known carrier for the c.994 C>T mutation.