Human L1CAM carrying the missense mutations of the fibronectin-like type III domains is localized in the endoplasmic reticulum and degraded by polyubiquitylation
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jnr.22695/fullpdf
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4. Disruption of the mouse L1 gene leads to malformations of the nervous system;Dahme;Nat Genet,1997
5. Pathological missense mutations of neural cell adhesion molecule L1 affect homophilic and heterophilic binding activities;De Angelis;EMBO J,1999
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