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Exome sequencing identifies truncating mutations in PRRT2... | ResearchHub
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Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
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Authors
Wan‐Jin Chen
15 more
Wan‐Jin Chen
•
Yu Lin
13 more
•
Zhi‐Ying Wu
Published
November 20, 2011
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Journal
Nature Genetics
Topics
Biology
Internal Medicine
Medicine
Psychiatry And Mental Health
Sanger Sequencing
Show all topics
DOI
10.1038/ng.1008
