Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Attention and IMMP2L[original query] |
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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Molecular psychiatry 2010 Jun 15 (6): 637-46. Elia J, Gai X, Xie H M, Perin J C, Geiger E, Glessner J T, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga B M, Wang L, Takeda T, Rappaport E F, Grant S F A, Berrettini W, Devoto M, Shaikh T H, Hakonarson H, White P |
Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome. European journal of human genetics : EJHG 2014 Nov 22 (11): 1283-9. Bertelsen Birgitte, Melchior Linea, Jensen Lars R, Groth Camilla, Glenthøj Birte, Rizzo Renata, Debes Nanette Mol, Skov Liselotte, Brøndum-Nielsen Karen, Paschou Peristera, Silahtaroglu Asli, Tümer Zeyn |
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