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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Detalles Bibliográficos
Autores principales: Reiner, Orly, Coquelle, Frédéric M, Peter, Bastian, Levy, Talia, Kaplan, Anna, Sapir, Tamar, Orr, Irit, Barkai, Naama, Eichele, Gregor, Bergmann, Sven
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550402/
https://www.ncbi.nlm.nih.gov/pubmed/16869982
http://dx.doi.org/10.1186/1471-2164-7-188

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550402/
https://www.ncbi.nlm.nih.gov/pubmed/16869982
http://dx.doi.org/10.1186/1471-2164-7-188

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