Cargando…
Altered RNA metabolism due to a homozygous RBM7 mutation in a patient with spinal motor neuropathy
The exosome complex is the most important RNA processing machinery within the cell. Mutations in its subunits EXOSC8 and EXOSC3 cause pontocerebellar hypoplasia, spinal muscular atrophy (SMA) and central nervous system demyelination. We present a patient with SMA-like phenotype carrying a homozygous...
Autores principales: | Giunta, Michele, Edvardson, Shimon, Xu, Yaobo, Schuelke, Markus, Gomez-Duran, Aurora, Boczonadi, Veronika, Elpeleg, Orly, Müller, Juliane S., Horvath, Rita |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5181591/ https://www.ncbi.nlm.nih.gov/pubmed/27193168 http://dx.doi.org/10.1093/hmg/ddw149 |
Ejemplares similares
-
EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia
por: Boczonadi, Veronika, et al.
Publicado: (2014) -
Genetic heterogeneity of motor neuropathies
por: Bansagi, Boglarka, et al.
Publicado: (2017) -
Mitochondria: Impaired mitochondrial translation in human disease
por: Boczonadi, Veronika, et al.
Publicado: (2014) -
Amyloid‐β in mitochondrial disease: mutation in a human metallopeptidase links amyloidotic neurodegeneration with mitochondrial processing
por: Boczonadi, Veronika, et al.
Publicado: (2016) -
Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy
por: Smith, Ian C., et al.
Publicado: (2023)