Cargando…
Unraveling the functional consequences of a novel germline missense mutation (R38C) in the yeast model of succinate dehydrogenase subunit B: insights into neurodegenerative disorders
This study explores the implications of a novel germline missense mutation (R38C) in the succinate dehydrogenase (SDH) subunit B, which has been linked to neurodegenerative diseases. The mutation was identified from the SDH mutation database and corresponds to the SDH2(R32C) allele, mirroring the hu...
Autores principales: | Zheng, Jiatong, Liu, Siru, Wang, Dongdong, Li, Linlin, Sarsaiya, Surendra, Zhou, Hua, Cai, Heng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568460/ https://www.ncbi.nlm.nih.gov/pubmed/37840772 http://dx.doi.org/10.3389/fnmol.2023.1246842 |
Ejemplares similares
-
Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD
por: Andrews, Katrina A, et al.
Publicado: (2018) -
Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene
por: Chen, Wen Min, et al.
Publicado: (2021) -
Correction: Tumour risks and genotype-phenotype correlations associated with germline variants in the succinate dehydrogenase subunit genes SDHB, SDHC, and SDHD
Publicado: (2019) -
Hereditary Pheochromocytoma With a Mutation in the Succinate Dehydrogenase Subunit A Gene
por: Karuppasamy, Gowri, et al.
Publicado: (2022) -
Succinate dehydrogenase variants in paraganglioma: why are B subunit variants ‘bad’?
por: Gruber, Lucinda M, et al.
Publicado: (2023)