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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...
Autores principales: | Reiner, Orly, Coquelle, Frédéric M, Peter, Bastian, Levy, Talia, Kaplan, Anna, Sapir, Tamar, Orr, Irit, Barkai, Naama, Eichele, Gregor, Bergmann, Sven |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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Materias: | |
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 |
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