Issa, F.A., Mock, A.F., Sagasti, A., and Papazian, D.M. (2012) Spinocerebellar ataxia type 13 mutation associated with disease onset in infancy disrupts axonal pathfinding during neuronal development. Dis. Model. Mech. epub 26 June 2012 doi: 10.1242/dmm.010157.
Minassian, N.A.*, Lin, M.A.*, and Papazian, D.M. (2012) Altered Kv3.3 channel gating in early onset spinocerebellar ataxia type 13. J. Physiol. 590.7, 1599-1614. (*equal contributors)
Issa, F.A., Mazzochi, C., Mock, A.F., and Papazian, D.M. (2011) Spinocerebellar ataxia type 13 mutant potassium channel alters neuronal excitability and causes locomotor deficits in zebrafish. J. Neurosci. 31, 6831-6841.
Link to my complete PubMed bibliography