Novel <it>PRRT2</it> mutation in an African-American family with paroxysmal kinesigenic dyskinesia
<p>Abstract</p> <p>Background</p> <p>Recently, heterozygous mutations in <it>PRRT2</it> (Chr 16p11.2) have been identified in Han Chinese, Japanese and Caucasians with paroxysmal kinesigenic dyskinesia. In previous work, a paroxysmal kinesigenic dyskinesia l...
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2012-09-01
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| Series: | BMC Neurology |
| Subjects: | |
| Online Access: | http://www.biomedcentral.com/1471-2377/12/93 |