Cargando…
Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency()
Multiple respiratory chain deficiencies represent a common cause of mitochondrial diseases and are associated with a wide range of clinical symptoms. We report a subject, born to consanguineous parents, with growth retardation and neurological deterioration. Multiple respiratory chain deficiency was...
Autores principales: | Serre, Valérie, Rozanska, Agata, Beinat, Marine, Chretien, Dominique, Boddaert, Nathalie, Munnich, Arnold, Rötig, Agnès, Chrzanowska-Lightowlers, Zofia M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Pub. Co
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787750/ https://www.ncbi.nlm.nih.gov/pubmed/23603806 http://dx.doi.org/10.1016/j.bbadis.2013.04.014 |
Ejemplares similares
-
Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit
por: Dennerlein, Sven, et al.
Publicado: (2010) -
Mitochondrial protein synthesis: Figuring the fundamentals, complexities and complications, of mammalian mitochondrial translation
por: Lightowlers, Robert N., et al.
Publicado: (2014) -
The human RNA-binding protein RBFA promotes the maturation of the mitochondrial ribosome
por: Rozanska, Agata, et al.
Publicado: (2017) -
Human mitochondrial ribosomes can switch structural tRNAs – but when and why?
por: Chrzanowska-Lightowlers, Zofia, et al.
Publicado: (2017) -
Structure based hypothesis of a mitochondrial ribosome rescue mechanism
por: Huynen, Martijn A, et al.
Publicado: (2012)