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Fragile X mental retardation protein controls ion channel expression and activity
Fragile X‐associated disorders are a family of genetic conditions resulting from the partial or complete loss of fragile X mental retardation protein (FMRP). Among these disorders is fragile X syndrome, the most common cause of inherited intellectual disability and autism. FMRP is an RNA‐binding pro...
Kaydedildi:
| Yayımlandı: | J Physiol |
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| Yazar: | |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5063927/ https://ncbi.nlm.nih.gov/pubmed/26864773 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/JP270675 |
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