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A quantitative homogeneous assay for fragile X mental retardation 1 protein
BACKGROUND: Hypermethylation of the fragile X mental retardation 1 gene FMR1 results in decreased expression of FMR1 protein FMRP, which is the underlying cause of Fragile X syndrome – an incurable neurological disorder characterized by mental retardation, anxiety, epileptic episodes and autism. Dis...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3635944/ https://ncbi.nlm.nih.gov/pubmed/23548045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-5-8 |
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