Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy

Haack, TB (author)

Ignatius, E (author)

Calvo-Garrido, J (author)

Karolinska Institutet

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Iuso, A (author)

Isohanni, P (author)

Maffezzini, C (author)

Karolinska Institutet

Lonnqvist, T (author)

Suomalainen, A (author)

Gorza, M (author)

Kremer, LS (author)

Graf, E (author)

Hartig, M (author)

Berutti, R (author)

Paucar, M (author)

Karolinska Institutet

Svenningsson, P (author)

Karolinska Institutet

Stranneheim, H (author)

Karolinska Institutet

Brandberg, G (author)

Wedell, A (author)

Karolinska Institutet

Kurian, MA (author)

Hayflick, SA (author)

Venco, P (author)

Tiranti, V (author)

Strom, TM (author)

Dichgans, M (author)

Horvath, R (author)

Holinski-Feder, E (author)

Freyer, C (author)

Karolinska Institutet

Meitinger, T (author)

Prokisch, H (author)

Senderek, J (author)

Wredenberg, A (author)

Karolinska Institutet

Carroll, CJ (author)

Klopstock, T (author)

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 (creator_code:org_t)

Elsevier BV, 2016

2016

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 99:3, s. 735-743

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https://doi.org/10.1...

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• Journal article (peer-reviewed)