Cargando…
Arterial hypertension in Leigh syndrome due to m.13513G > A is multicausal, requiring an extensive search to identify its pathphysiology
Autor principal: | Finsterer, Josef |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314592/ https://www.ncbi.nlm.nih.gov/pubmed/37391837 http://dx.doi.org/10.1186/s40885-023-00247-4 |
Ejemplares similares
-
Adult-Onset Leigh Syndrome Due to an m.13513G>A Mutation
por: Hirosawa, Hiroaki, et al.
Publicado: (2021) -
Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes/Leigh Overlap Syndrome Due to Variant m.13513G>A in MT-ND5
por: Finsterer, Josef, et al.
Publicado: (2022) -
MELAS with multiple stroke‐like episodes due to the variant m.13513G>A in MT‐ND5
por: Ghosh, Ritwik, et al.
Publicado: (2022) -
Case Report: m.13513 G>A Mutation in a Chinese Patient With Both Leigh Syndrome and Wolff-Parkinson-White Syndrome
por: Liang, Jian-Min, et al.
Publicado: (2021) -
Commentary: Case report: Optic atrophy and nephropathy with m.13513G>A/MT-ND5 mtDNA pathogenic variant
por: Finsterer, Josef
Publicado: (2022)