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Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficiency mice
CYFIP1 maps to the interval between proximal breakpoint 1 (BP1) and breakpoint 2(AS) and Prader-Willi syndrome. There is only one breakpoint (BP3) at the distal end of deletion. CYFIP1 is deleted in AS patients with the larger class I deletion (BP1 to BP3) and the neurological presentations in these...
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| Publicado no: | Brain Res |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4744651/ https://ncbi.nlm.nih.gov/pubmed/26474913 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2015.10.015 |
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