Identification of a functional rare variant in autism using...

Human Molecular Genetics 2011 / 09 Vol. 20; Iss. 18

Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression

Ben-David, E., Granot-Hershkovitz, E., Monderer-Rothkoff, G., Lerer, E., Levi, S., Yaari, M., Ebstein, R. P., Yirmiya, N., Shifman, S.
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Volume:
20
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddr283
Date:
September, 2011
File:
PDF, 330 KB
english, 2011
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