Next generation sequencing for neurological diseases: New hope or new hype?

por Keogh, M.J., Chinnery, P.F.
Publicado 2013

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 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 2016