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Rare copy number variants in NRXN1 and CNTN6 increase ris... | ResearchHub
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Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome
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Authors
Alden Huang
70 more
Alden Huang
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Alden Huang
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Giovanni Coppola
Published
July 8, 2016
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Preprint Server
Topics
Biology
Genetics And Genomics
Medicine
Genetics
Copy-Number Variation
Show all topics
DOI
10.1101/062471
License
CC-BY-NC-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Medicine
Genetics
Copy-Number Variation
Show all topics
DOI
10.1101/062471
License
CC-BY-NC-ND
Other Formats
PDF
