A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking

Khare, S (author)

Nick, JA (author)

Zhang, YL (author)

Galeano, K (author)

Butler, B (author)

Khoshbouei, H (author)

Rayaprolu, S (author)

Hathorn, T (author)

Ranum, LPW (author)

Smithson, L (author)

Golde, TE (author)

Morse, R (author)

Raff, M (author)

Simon, J (author)

Ld, MNE (author)

Rincon-Limas, DE (author)

Lewis, J (author)

Kaczmarek, LK (author)

Fernandez-Funez, P (author)

Nick, HS (author)

Waters, MF (author)

(creator_code:org_t)

2017-05-03
2017
English.
In: PloS one. - : Public Library of Science (PLoS). - 1932-6203. ; 12:5, s. e0173565-

Related links:: https://journals.plo...; show more...; http://kipublication...; https://doi.org/10.1...; show less...

Subject headings

By the author/editor: Khare, S; Nick, JA; Zhang, YL; Galeano, K; Butler, B; Khoshbouei, H; show more...; Rayaprolu, S; Hathorn, T; Ranum, LPW; Smithson, L; Golde, TE; Paucar, M; Morse, R; Raff, M; Simon, J; Ld, MNE; Wirdefeldt, K; Rincon-Limas, DE; Lewis, J; Kaczmarek, LK; Fernandez-Funez, ...; Nick, HS; Waters, MF; show less...

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