Braun, R., Gloeckner, C., Kinkl, N., Kolch, W., Meitinger, T., O'Neill, E., Prokisch, H., Schumacher, A. and Ueffing, M. (2006) The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity. Human Molecular Genetics, 15(2), pp. 223-232.
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Item Type: | Articles |
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Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | Kolch, Prof Walter |
Authors: | Braun, R., Gloeckner, C., Kinkl, N., Kolch, W., Meitinger, T., O'Neill, E., Prokisch, H., Schumacher, A., and Ueffing, M. |
College/School: | College of Medical Veterinary and Life Sciences |
Journal Name: | Human Molecular Genetics |
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