A case of an African American man with ataxia and oculomotor apraxia 2

J Clin Neuromuscul Dis. 2014 Sep;16(1):43-6. doi: 10.1097/CND.0000000000000042.

Authors

Bhavesh Trikamji¹, Nicholas Parziale, Nastaran Rafiei, Robert Freundlich, Shri Mishra

Affiliation

¹ *Department of Neurology, Olive View UCLA Medical Center, Sylmar, CA †Department of Neurology, VA Greater Los Angeles HCS, Los Angeles, CA ‡Department of Neurology, UCLA David Geffen School of Medicine, Los Angeles, CA §Department of Neurology, USC Keck School of Medicine, Los Angeles, CA ¶Department of Neurology, UCLA David Geffen School of Medicine, Los Angeles, CA ‖Department of Neurology, Olive View UCLA Medical Center, Sylmar, CA.

PMID: 25137517
DOI: 10.1097/CND.0000000000000042

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Apraxias / congenital
Ataxia / complications*
Ataxia / genetics
Black or African American
Cogan Syndrome / complications*
Cogan Syndrome / genetics
DNA Helicases
Humans
Magnetic Resonance Imaging
Male
Multifunctional Enzymes
Mutation / genetics
RNA Helicases / genetics

Substances

Multifunctional Enzymes
SETX protein, human
DNA Helicases
RNA Helicases

Supplementary concepts

Apraxia, oculomotor, Cogan type