Cargando…
MLASA-1: A Rare Cause of Myopathy with Sideroblastic Anemia
Autores principales: | Sait, Benazer, Chidambaram, Aakash C., Dinesh Babu, R. M., Vidhyasagar, Krishnamoorthy, Xavier, Joshua R., Sagayaraj, Benjamin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996516/ https://www.ncbi.nlm.nih.gov/pubmed/36911436 http://dx.doi.org/10.4103/aian.aian_661_22 |
Ejemplares similares
-
Myopathy, lactic acidosis and sideroblastic anemia 1 (MLASA1): A 25-year follow-up
por: Woods, Jeremy, et al.
Publicado: (2019) -
A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations
por: Shahni, Rojeen, et al.
Publicado: (2013) -
A Myopathy, Lactic Acidosis, Sideroblastic Anemia (MLASA) Case Due to a Novel PUS1 Mutation
por: Kasapkara, Çiğdem Seher, et al.
Publicado: (2017) -
Causes and Pathophysiology of Acquired Sideroblastic Anemia
por: Rodriguez-Sevilla, Juan Jose, et al.
Publicado: (2022) -
The phenotypic spectrum of germline YARS2 variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2
por: Riley, Lisa G., et al.
Publicado: (2018)