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

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

scientific article published on 3 May 2017

Author/s

author: Sruti Rayaprolu, Magnus Nordenskjöld, Karin Wirdefeldt, Laura Ranum

Work details

Publication date

May 3, 2017

Language

English

Copyright status

copyrighted