Cargando…
A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy
Aminoacyl-tRNA synthetases (ARSs) are essential enzymes with a critical role in protein synthesis: charging tRNA molecules with cognate amino acids. Heterozygosity for variants in five genes (AARS1, GARS1, HARS1, WARS1, and YARS1) encoding cytoplasmic, dimeric ARSs have been associated with autosoma...
Autores principales: | Forrest, Megan E., Meyer, Alayne P., Laureano Figueroa, Stephanie M., Antonellis, Anthony |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808560/ https://www.ncbi.nlm.nih.gov/pubmed/36307205 http://dx.doi.org/10.1101/mcs.a006246 |
Ejemplares similares
-
A Novel Homozygous Missense Mutation in the YARS Gene: Expanding the Phenotype of YARS Multisystem Disease
por: Zeiad, Rawah K H M, et al.
Publicado: (2021) -
YARS2 Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality
por: Gurtner, Corinne, et al.
Publicado: (2020) -
The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype
por: Averdunk, Luisa, et al.
Publicado: (2021) -
Maternal mosaicism for a missense variant in the SMS gene that causes Snyder–Robinson syndrome
por: Marhabaie, Mohammad, et al.
Publicado: (2021) -
Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia
por: Riley, Lisa G, et al.
Publicado: (2013)