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A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking
Document Type
Artikel
Author
Khare, S; Nick, JA; Zhang, YL; Galeano, K; Butler, B; Khoshbouei, H; 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, P; Nick, HS; Waters, MF
Source
PloS one. 12(5):e0173565
Subject
Medicin och hälsovetenskap
Language
English
English
ISSN
1932-6203

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