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A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1 by Yi Bessie Liu, Ambika Tewari, Johnny Salameh, Elena Arystarkhova, Thomas G Hampton, Allison Brashear, Laurie J Ozelius, Kamran Khodakhah, Kathleen J Sweadner
Published 2015-12-01
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Reduction of thalamic and cortical Ih by deletion of TRIP8b produces a mouse model of human absence epilepsy by Robert J. Heuermann, Thomas C. Jaramillo, Shui-Wang Ying, Benjamin A. Suter, Kyle A. Lyman, Ye Han, Alan S. Lewis, Thomas G. Hampton, Gordon M.G. Shepherd, Peter A. Goldstein, Dane M. Chetkovich
Published 2016-01-01
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