Cargando…
Mitochondrial respiratory chain dysfunction in a patient with a heterozygous de novo CTBP1 variant
The C‐terminal binding protein 1 (CTBP1) functions as a transcriptional corepressor in vertebrates and has been identified to have critical roles in nervous system growth and development. Pathogenic variants in the CTBP1 gene has been shown to cause hypotonia, ataxia, developmental delay and tooth e...
Autores principales: | Wong, Wui‐Kwan, Balasubramaniam, Shanti, Wong, Rachel S. H., Graf, Nicole, Thorburn, David R., McFarland, Robert, Troedson, Christopher |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626656/ https://www.ncbi.nlm.nih.gov/pubmed/36341169 http://dx.doi.org/10.1002/jmd2.12326 |
Ejemplares similares
-
De novo CTBP1 variant is associated with decreased mitochondrial respiratory chain activities
por: Sommerville, Ewen W., et al.
Publicado: (2017) -
Compound heterozygous mutations in glycyl-tRNA synthetase (GARS) cause mitochondrial respiratory chain dysfunction
por: Nafisinia, Michael, et al.
Publicado: (2017) -
Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in
AFG3L2
por: Wong, Wui‐Kwan, et al.
Publicado: (2022) -
CTBP1 and CTBP2 mutations underpinning neurological disorders: a systematic review
por: Acosta-Baena, Natalia, et al.
Publicado: (2022) -
Steroid‐responsive aseptic meningitis with raised intracranial pressure syndrome associated with myelin oligodendrocyte glycoprotein autoantibodies
por: Wong, Wui‐Kwan, et al.
Publicado: (2022)