Muto, V; Flex, E; Kupchinsky, Z; Primiano, G; Galehdari, H; Dehghani, M; Cecchetti, S; Carpentieri, G; Rizza, T; Mazaheri, N; et al. Muto, V; Flex, E; Kupchinsky, Z; Primiano, G; Galehdari, H; Dehghani, M; Cecchetti, S; Carpentieri, G; Rizza, T; Mazaheri, N; Sedaghat, A; Mehrjardi, M; Traversa, A; Di Nottia, M; Kousi, M; Jamshidi, Y; Ciolfi, A; Caputo, V; Malamiri, R; Pantaleoni, F; Martinelli, S; Jeffries, A; Zeighami, J; Sherafat, A; Di Giuda, D; Shariati, G; Carrozzo, R; Katsanis, N; Maroofian, R; Servidei, S; Tartaglia, M (2019) Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration. In: 51st European Society of Human Genetics Conference, EUROPEAN JOURNAL OF HUMAN GENETICS, June 16-19th 2018, Milan.
SGUL Authors: Jamshidi, Yalda

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Item Type:	Conference or Workshop Item (Poster)
Additional Information:	This is a post-peer-review, pre-copyedit version of an article published in European Journal of Human Genetics. The final authenticated version is available online at: http://dx.doi.org/10.1038/s41431-019-0404-7
Keywords:	0604 Genetics, Genetics & Heredity
SGUL Research Institute / Research Centre:	Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title:	EUROPEAN JOURNAL OF HUMAN GENETICS
Article Number:	P09.142B
ISSN:	1018-4813
Related URLs:	Organisation
Dates:	Date Event 3 July 2019 Published
Publisher License:	Publisher's own licence
Web of Science ID:	WOS:000489313102167
URI:	https://openaccess.sgul.ac.uk/id/eprint/111323

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