The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

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
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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