Cargando…
Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome
Carriers of the fragile X premutation (FPM) have CGG trinucleotide repeat expansions of between 55 and 200 in the 5′-UTR of FMR1, compared to a CGG repeat length of between 5 and 54 for the general population. Carriers were once thought to be without symptoms, but it is now recognized that they can...
Autores principales: | Berman, Robert F, Buijsen, Ronald AM, Usdin, Karen, Pintado, Elizabeth, Kooy, Frank, Pretto, Dalyir, Pessah, Isaac N, Nelson, David L, Zalewski, Zachary, Charlet-Bergeurand, Nicholas, Willemsen, Rob, Hukema, Renate K |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135345/ https://www.ncbi.nlm.nih.gov/pubmed/25136376 http://dx.doi.org/10.1186/1866-1955-6-25 |
Ejemplares similares
-
FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome
por: Buijsen, Ronald AM, et al.
Publicado: (2014) -
BC RNA Mislocalization in the Fragile X Premutation
por: Muslimov, Ilham A., et al.
Publicado: (2018) -
The multiple molecular facets of fragile X-associated tremor/ataxia syndrome
por: Sellier, Chantal, et al.
Publicado: (2014) -
Fragile X Premutation
por: Tassone, Flora, et al.
Publicado: (2014) -
FMR1 premutation with Prader–Willi phenotype and fragile X‐associated tremor/ataxia syndrome
por: Martínez‐Cerdeño, Verónica, et al.
Publicado: (2017)