Onset of MELAS due to the m.3243A>G mutation is early if the large phenotypic variability is considered
Main Authors: | Josef Finsterer, Sinda Zarrouk-Mahjoub |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2017-03-01
|
Series: | Molecular Genetics and Metabolism Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S221442691630132X |
Similar Items
-
Late-onset mitochondrial encephalomyopathy with lactic acid and stroke-like episodes (MELAS), defining symptomology
by: J. Gass, et al.
Published: (2017-03-01) -
Optimising therapeutic strategies for acute stroke-like lesions in MELAS
by: Josef Finsterer
Published: (2020-12-01) -
mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease
by: John P Grady, et al.
Published: (2018-06-01) -
Evaluación de la mutación a3243g en mtDNA, en familias de pacientes diagnosticados con el síndrome Melas Clinical characteristics of vesicoureteral Reflux in children at a University Hospital in Medellín, Colombia. 1960-2004.
by: Andrés Ruiz, et al.
Published: (2003-01-01) -
Commentary: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL1 m.3243A>G point mutation: neuroradiological features and their implications for underlying pathogenesis
by: Josef Finsterer, et al.
Published: (2023-04-01)