Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia

Por Keogh, M. J., Steele, H., Douroudis, K., Pyle, A., Duff, J., Hussain, R., Smertenko, T., Griffin, H., Santibanez-Koref, M., Horvath, R., Chinnery, P. F.
Publicado no J Neurol (2015)

Exome sequencing in dementia with Lewy bodies

Por Keogh, M J, Kurzawa-Akanbi, M, Griffin, H, Douroudis, K, Ayers, K L, Hussein, R I, Hudson, G, Pyle, A, Cordell, H J, Attems, J, McKeith, I G, O'Brien, J T, Burn, D J, Morris, C M, Thomas, A J, Chinnery, P F
Publicado no Transl Psychiatry (2016)