A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect
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| Description | scientific article published in Journal of Biological Chemistry |
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author: Bettina Winckler Chan Choo Yap |
| Publication date | October 5, 2018 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |