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Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants
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- Halvorsen, M (author)
- Karolinska Institutet
- Samuels, J (author)
- Wang, Y (author)
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- Greenberg, BD (author)
- Fyer, AJ (author)
- McCracken, JT (author)
- Geller, DA (author)
- Knowles, JA (author)
- Zoghbi, AW (author)
- Pottinger, TD (author)
- Grados, MA (author)
- Riddle, MA (author)
- Bienvenu, OJ (author)
- Nestadt, PS (author)
- Krasnow, J (author)
- Goes, FS (author)
- Maher, B (author)
- Nestadt, G (author)
- Goldstein, DB (author)
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- (creator_code:org_t)
- 2021-06-28
- 2021
- English.
- In: Nature neuroscience. - : Springer Science and Business Media LLC. - 1546-1726 .- 1097-6256. ; 24:8, s. 1071-1076
- Journal article (peer-reviewed)
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- Halvorsen, M
- Samuels, J
- Wang, Y
- Greenberg, BD
- Fyer, AJ
- McCracken, JT
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- Geller, DA
- Knowles, JA
- Zoghbi, AW
- Pottinger, TD
- Grados, MA
- Riddle, MA
- Bienvenu, OJ
- Nestadt, PS
- Krasnow, J
- Goes, FS
- Maher, B
- Nestadt, G
- Goldstein, DB
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