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Exome Sequencing of Familial Bipolar Disorder.

Goes, Fernando S (author)
Pirooznia, Mehdi (author)
Parla, Jennifer S (author)
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Kramer, Melissa (author)
Ghiban, Elena (author)
Mavruk, Senem (author)
Chen, Yun-Ching (author)
Monson, Eric T (author)
Willour, Virginia L (author)
Karchin, Rachel (author)
Flickinger, Matthew (author)
Locke, Adam E (author)
Levy, Shawn E (author)
Scott, Laura J (author)
Boehnke, Michael (author)
Stahl, Eli (author)
Moran, Jennifer L (author)
Karolinska Institutet
Hultman, Christina M (author)
Karolinska Institutet
Landén, Mikael, 1966 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology
Purcell, Shaun M (author)
Sklar, Pamela (author)
Zandi, Peter P (author)
McCombie, W Richard (author)
Potash, James B (author)
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 (creator_code:org_t)
American Medical Association (AMA), 2016
2016
English.
In: JAMA psychiatry. - : American Medical Association (AMA). - 2168-6238 .- 2168-622X. ; 73:6, s. 590-7
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Complex disorders, such as bipolar disorder (BD), likely result from the influence of both common and rare susceptibility alleles. While common variation has been widely studied, rare variant discovery has only recently become feasible with next-generation sequencing.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Psykiatri (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Psychiatry (hsv//eng)

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