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Protein Implicated in Nonsyndromic Mental Retardation Regulates Protein Kinase A (PKA) Activity
Mutation of the coiled-coil and C2 domain-containing 1A (CC2D1A) gene, which encodes a C2 domain and DM14 domain-containing protein, has been linked to severe autosomal recessive nonsyndromic mental retardation. Using a mouse model that produces a truncated form of CC2D1A that lacks the C2 domain an...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3340277/ https://ncbi.nlm.nih.gov/pubmed/22375002 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.261875 |
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