Items where Author is "Singleton, AB"

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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)

Kara, E and Tucci, A and Manzoni, C and Lynch, DS and Elpidorou, M and Bettencourt, C and Chelban, V and Manole, A and Hamed, S and Federoff, M and Preza, E and Hughes, D and Pittman, A and Jaunmuktane, Z and Brandner, S and Xiromerisiou, G and Wiethoff, S and Schottlaender, L and Proukakis, C and Morris, HW and Warner, T and Bhatia, KP and Korlipara, P and Singleton, AB and Hardy, J and Wood, NW and Lewis, PA And Houlden, H (2016) Genetic and phenotypic characterisation of complex hereditary spastic paraplegia. BRAIN, 139 (7). pp. 1904-1918.

This list was generated on Wed Oct 20 07:42:09 2021 BST.