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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Detalles Bibliográficos
Autores principales: Schutzius, Gabi, Bleckmann, Dorothee, Kapps-Fouthier, Sandra, di Giorgio, Francesco, Gerhartz, Bernd, Weiss, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
New Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635944/
https://www.ncbi.nlm.nih.gov/pubmed/23548045
http://dx.doi.org/10.1186/1866-1955-5-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635944/
https://www.ncbi.nlm.nih.gov/pubmed/23548045
http://dx.doi.org/10.1186/1866-1955-5-8

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