Items where Author is "Ryten, M"

Up a level
Export as [feed] Atom [feed] RSS
Group by: Item Type | No Grouping
Jump to: Article | Other
Number of items: 2.

Article

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.

Other

Soutar, MPM and Melandri, D and Annuario, E and Monaghan, AE and Welsh, NJ and D’Sa, K and Guelfi, S and Zhang, D and Pittman, A and Trabzuni, D and Pan, KS and Kia, DA and Bictash, M and Gandhi, S and Houlden, H and Cookson, MR and Wood, NW and Singleton, AB and Hardy, J and Whiting, PJ and Blauwendraat, C and Whitworth, AJ and Manzoni, C and Ryten, M and Lewis, PA and Plun-Favreau, H (2020) Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson’s disease at Chr16q11.2 and on the MAPT H1 allele. Cold Spring Harbor Laboratory. (Submitted)

This list was generated on Tue Dec 1 07:19:43 2020 GMT.