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Exome sequencing in...
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Halvorsen, MKarolinska Institutet
(author)
Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants
- Article/chapterEnglish2021
Publisher, publication year, extent ...
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2021-06-28
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Springer Science and Business Media LLC,2021
Numbers
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LIBRIS-ID:oai:prod.swepub.kib.ki.se:147026200
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http://kipublications.ki.se/Default.aspx?queryparsed=id:147026200URI
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https://doi.org/10.1038/s41593-021-00876-8DOI
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Added entries (persons, corporate bodies, meetings, titles ...)
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Samuels, J
(author)
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Wang, Y
(author)
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Greenberg, BD
(author)
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Fyer, AJ
(author)
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McCracken, JT
(author)
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Geller, DA
(author)
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Knowles, JA
(author)
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Zoghbi, AW
(author)
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Pottinger, TD
(author)
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Grados, MA
(author)
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Riddle, MA
(author)
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Bienvenu, OJ
(author)
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Nestadt, PS
(author)
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Krasnow, J
(author)
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Goes, FS
(author)
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Maher, B
(author)
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Nestadt, G
(author)
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Goldstein, DB
(author)
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Karolinska Institutet
(creator_code:org_t)
Related titles
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In:Nature neuroscience: Springer Science and Business Media LLC24:8, s. 1071-10761546-17261097-6256
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Halvorsen, M
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Samuels, J
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Wang, Y
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Greenberg, BD
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Fyer, AJ
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McCracken, JT
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show more...
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Geller, DA
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Knowles, JA
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Zoghbi, AW
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Pottinger, TD
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Grados, MA
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Riddle, MA
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Bienvenu, OJ
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Nestadt, PS
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Krasnow, J
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Goes, FS
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Maher, B
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Nestadt, G
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Goldstein, DB
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Nature neuroscie ...
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Karolinska Institutet