Cargando…
A homozygous POLR1A variant causes leukodystrophy and affects protein homeostasis
RNA polymerase I transcribes ribosomal DNA to produce precursor 47S rRNA. Post-transcriptional processing of this rRNA generates mature 28S, 18S and 5.8S rRNAs, which form the ribosomes, together with 5S rRNA, assembly factors and ribosomal proteins. We previously reported a homozygous variant in th...
Autores principales: | Misceo, Doriana, Lirussi, Lisa, Strømme, Petter, Sumathipala, Dulika, Guerin, Andrea, Wolf, Nicole I, Server, Andres, Stensland, Maria, Dalhus, Bjørn, Tolun, Aslıhan, Kroes, Hester Y, Nyman, Tuula A, Nilsen, Hilde L, Frengen, Eirik |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393412/ https://www.ncbi.nlm.nih.gov/pubmed/36917474 http://dx.doi.org/10.1093/brain/awad086 |
Ejemplares similares
-
Sudden death in epilepsy and ectopic neurohypophysis in Joubert syndrome 23 diagnosed using SNVs/indels and structural variants pipelines on WGS data: a case report
por: Sumathipala, Dulika, et al.
Publicado: (2020) -
POLR3-related Leukodystrophy
por: Thomas, Aby, et al.
Publicado: (2019) -
4H leukodystrophy caused by a homozygous POLR3B mutation: Further delineation of the phenotype
por: Verberne, Eline A., et al.
Publicado: (2020) -
Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
por: Pedurupillay, Christeen Ramane J., et al.
Publicado: (2016) -
Craniofacial features of POLR3-related leukodystrophy caused by biallelic variants in POLR3A, POLR3B and POLR1C
por: Mirchi, Amytice, et al.
Publicado: (2023)