The evolving doublecortin (DCX) superfamily

BACKGROUND: Doublecortin (DCX) domains serve as protein-interaction platforms. Mutations in members of this protein superfamily are linked to several genetic diseases. Mutations in the human DCX gene result in abnormal neuronal migration, epilepsy, and mental retardation; mutations in RP1 are associ...

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Detalhes bibliográficos
Main Authors: Reiner, Orly, Coquelle, Frédéric M, Peter, Bastian, Levy, Talia, Kaplan, Anna, Sapir, Tamar, Orr, Irit, Barkai, Naama, Eichele, Gregor, Bergmann, Sven
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2006
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1550402/
https://ncbi.nlm.nih.gov/pubmed/16869982
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-7-188
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