Cargando…
MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
[Image: see text]
Autores principales: | Gal, Aniko, Balicza, Peter, Weaver, David, Naghdi, Shamim, Joseph, Suresh K, Várnai, Péter, Gyuris, Tibor, Horváth, Attila, Nagy, Laszlo, Seifert, Erin L, Molnar, Maria Judit, Hajnóczky, György |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405051/ https://www.ncbi.nlm.nih.gov/pubmed/37431817 http://dx.doi.org/10.15252/emmm.202317911 |
Ejemplares similares
-
MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
por: Gal, Aniko, et al.
Publicado: (2017) -
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
por: Nasca, Alessia, et al.
Publicado: (2017) -
Answer to Gerber et al. “Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy”
por: Gál, Anikó, et al.
Publicado: (2023) -
Novel biallelic variants in MSTO1 associated with mitochondrial myopathy
por: Schultz-Rogers, Laura, et al.
Publicado: (2019) -
Indentification of novel MSTO1 compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxia
por: Chen, Jia, et al.
Publicado: (2022)