Haack, T., Ignatius, E., Calvo-Garrido, J., Iuso, A., Isohanni, P., Maffezzini, C., . . . Klopstock, T. (2016). Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy. Am J Hum Genet.
Citação norma ChicagoHaack, Tobias B., et al. "Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration With Ataxia, Dystonia, and Gaze Palsy." Am J Hum Genet 2016.
Deismireacht MLAHaack, Tobias B., et al. "Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration With Ataxia, Dystonia, and Gaze Palsy." Am J Hum Genet 2016.
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