Items where Author is "Morris, H R"

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Article

Kiely, A P and Ling, H and Asi, Y T and Kara, E and Proukakis, C and Schapira, A H and Morris, H R and Lubbe, S and Limousin, P and Lewis, P A and Lees, A J and Quinn, N and Hardy, J and Love, S and Revesz, T and Houlden, H and Holton, J L (2015) Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation. Molecular Neurodegeneration, 10. p. 41.

Mencacci, N E and Rubio-Agusti, I and Zdebik, A and Asmus, F and Ludtmann, M H R and Ryten, M and Plagnol, V and Hauser, A K and Bandres-Ciga, S and Bettencourt, C and Forabosco, P and Hughes, D and Soutar, M M and Peall, K and Morris, H R and Trabzuni, D and Tekman, M and Stanescu, H C and Kleta, R and Carecchio, M and Zorzi, G and Nardocci, N and Garavaglia, B and Lohmann, E and Weissbach, A and Klein, C and Hardy, J and Pittman, A M and Foltynie, T and Abramov, A Y and Gasser, T and Bhatia, K P and Wood, N W (2015) A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia. American Journal of Human Genetics, 96 (6). pp. 938-47.

This list was generated on Mon Dec 6 07:30:11 2021 GMT.