Identification of the Kelch Family Protein Nd1-L as a Novel Molecular Interactor of KRIT1

Loss-of-function mutations of the KRIT1 gene (CCM1) have been associated with the Cerebral Cavernous Malformation (CCM) disease, which is characterized by serious alterations of brain capillary architecture. The KRIT1 protein contains multiple interaction domains and motifs, suggesting that it might...

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מידע ביבליוגרפי
Main Authors: Guazzi, Paolo, Goitre, Luca, Ferro, Elisa, Cutano, Valentina, Martino, Chiara, Trabalzini, Lorenza, Retta, Saverio Francesco
פורמט: Artigo
שפה:Inglês
יצא לאור: Public Library of Science 2012
נושאים:
Research Article
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC3435375/
https://ncbi.nlm.nih.gov/pubmed/22970292
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0044705
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