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

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

DOI Full Paper Access

10

Citations

32

References

2018

Year

Chan Choo Yap, Laura Digilio, Kamil Kruczek, Matylda Roszkowska, Xiaoqin Fu, Judy S. Liu, Bettina Winckler

Journal of Biological Chemistry

Genetic DisorderEndocytosis DefectGeneticsDisease-associated G253d MutationMolecular BiologyDegenerative DiseaseDominant Dendrite PhenotypeMedicineCell Biology

References

	Year	Citations

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