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A neuronal function of the tumor suppressor protein merlin
Mutagenic loss of the NF2 tumor suppressor gene encoded protein merlin is known to provoke the hereditary neoplasia syndrome, Neurofibromatosis type 2 (NF2). In addition to glial cell-derived tumors in the PNS and CNS, disease-related lesions also affect the skin and the eyes. Furthermore, 60% of NF...
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Autori principali: | , , |
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Natura: | Artigo |
Lingua: | Inglês |
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BioMed Central
2014
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Soggetti: | |
Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4149232/ https://ncbi.nlm.nih.gov/pubmed/25012216 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-014-0082-1 |
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