Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.
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| Title: | Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression. |
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| Authors: | Ben-David E; Department of Genetics, The Institute of Life Sciences, The Hebrew University of Jerusalem,Edmond J. Safra campus, Jerusalem 91904, Israel., Granot-Hershkovitz E, Monderer-Rothkoff G, Lerer E, Levi S, Yaari M, Ebstein RP, Yirmiya N, Shifman S |
| Source: | Human molecular genetics [Hum Mol Genet] 2011 Sep 15; Vol. 20 (18), pp. 3632-41. Date of Electronic Publication: 2011 Jun 16. |
| Publication Type: | Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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