Cargando…
CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy‐like Phenotype
Autores principales: | Dewan, Ramita, Jaunmuktane, Zane, Garcia‐Segura, Monica Emili, Strand, Catherine, Wild, Edward, Villar, Joaquin, Dalgard, Clifton L., Tabrizi, Sarah J., Traynor, Bryan J., Proukakis, Christos |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308656/ https://www.ncbi.nlm.nih.gov/pubmed/35510647 http://dx.doi.org/10.1002/mds.29035 |
Ejemplares similares
-
Identification of multiple system atrophy mimicking Parkinson’s disease or progressive supranuclear palsy
por: Miki, Yasuo, et al.
Publicado: (2021) -
MAPT
‐Associated Familial Progressive Supranuclear Palsy with Typical Corticobasal Degeneration Neuropathology: A Clinicopathological Report
por: Cullinane, Patrick W., et al.
Publicado: (2023) -
Problems and solutions for the analysis of somatic CAG repeat expansion and their relationship to Huntington's disease toxicity
por: Budworth, Helen, et al.
Publicado: (2016) -
Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome
por: Jabbari, Edwin, et al.
Publicado: (2020) -
Zolpidem in Progressive Supranuclear Palsy
por: Dash, Sandip K.
Publicado: (2013)