A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect.

Journal: Journal of Biological Chemistry

Published: 2018-10-05

DOI: 10.1074/jbc.ra118.004462

Affiliations: 4

Authors: 7

Go to article
Institutions FC
Department of Cell Biology, UVA, United States of America (USA) 0.43
Department of Neurology, Brown University, United States of America (USA) 0.29
Faculty of Biochemistry, Biophysics and Biotechnology (WBBIB), UJ, Poland 0.14
Faculty of Biology and Earth Sciences, UJ, Poland 0.14