Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotype.

Neurobiology of aging - 1 Jan 2021

Liao Nai-Yi, Liao Kwong-Kum, Liao Yi-Chu, Lee Yi-Chung

Abstract excerpt

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) are 2 monogenic cerebral small vessel diseases sharing several common clinical features including young stroke, migraine, and cognitive dysfunction. The aim of this study was to understand the role of MELAS in patients with...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA, Mitochondrial
Share to CADASIL
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to MELAS Syndrome

Share to Mutation

Share to Phenotype

Source

Identifiers

PMID: 32950272
DOI: 10.1016/j.neurobiolaging.2020.08.016

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotype.PMID 32950272Read ↗

Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort.Semantic proximity Read ↗

Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.Semantic proximity Read ↗

A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL.Semantic proximity Read ↗

When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?Semantic proximity Read ↗

Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome: A case-report and literature review (CARE-complaint).Semantic proximity Read ↗

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?Semantic proximity Read ↗

Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation.Semantic proximity Read ↗

Uncommon mutation in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).Semantic proximity Read ↗

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.Semantic proximity Read ↗

Elderly Onset Male MELAS: A Case ReportSemantic proximity Read ↗

Neuromuscular implications in CADASIL.Semantic proximity Read ↗

Clinical features of MELAS and mitochondrial DNA mutations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.