[Skip to Content]
[Skip to Content Landing]

The patient was heterozygous for the Trp279* and Lys197Gln mutation in the APTX gene at 28 years of age. Cerebellar ataxia at gait and dysmetria during the finger-nose test were noted.

JN Learning™ is the home for CME and MOC from the JAMA Network. Search by specialty or US state and earn AMA PRA Category 1 Credit(s)™ from articles, audio, Clinical Challenges and more. Learn more about CME/MOC

Close
Close

Name Your Search

Save Search
Close
Close

Lookup An Activity

or

My Saved Searches

You currently have no searches saved.

Close

My Saved Courses

You currently have no courses saved.

Close