Yoon, G., Westmacott, R., MacMillan, L., Quercia, N., Koutsou, P., Georghiou, A., . . . Banwell, B. (2009). Complete deletion of the aprataxin gene: Ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficit. BMJ Publishing Group.

Yoon, Grace, Robyn Westmacott, Lynn MacMillan, Nada Quercia, Pantelitsa Koutsou, Anthi Georghiou, Kyproula Christodoulou, och Brenda Banwell. Complete Deletion of the Aprataxin Gene: Ataxia With Oculomotor Apraxia Type 1 With Severe Phenotype and Cognitive Deficit. BMJ Publishing Group, 2009.

Yoon, Grace, et al. Complete Deletion of the Aprataxin Gene: Ataxia With Oculomotor Apraxia Type 1 With Severe Phenotype and Cognitive Deficit. BMJ Publishing Group, 2009.