Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration

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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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Official URL: https://doi.org/10.1038/s41431-019-0404-7

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

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