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

Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A).

Journal of the peripheral nervous system : JPNS - 1 Sept 2009

Sole Guilhem, Ferrer Xavier, Vital Claude, Martin-Negrier Marie-Laure, Vital Anne, Latour Philippe

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Charcot-Marie-Tooth Disease
Share to Child
Share to GTP Phosphohydrolases
Share to Membrane Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mitochondria

Share to Mitochondrial Proteins

Share to Mutation

Source

Identifiers

PMID: 19909486
DOI: 10.1111/j.1529-8027.2009.00234.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A).PMID 19909486Read ↗

Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT.Semantic proximity Read ↗

CMT2A-linked MFN2 mutation, T206I promotes mitochondrial hyperfusion and predisposes cells towards mitophagy.Semantic proximity Read ↗

A human mitofusin 2 mutation causes mitophagic cardiomyopathySemantic proximity Read ↗

A human mitofusin 2 mutation can cause mitophagic cardiomyopathy.Semantic proximity Read ↗

The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy.Semantic proximity Read ↗

Quantifying Mitochondrial Dynamics in Patient Fibroblasts with Multiple Developmental Defects and Mitochondrial Disorders.Semantic proximity Read ↗

A novel variant in MFN2 linked to a lethal disorder of neonatal onsetSemantic proximity Read ↗

The Spectrum of Mitochondrial Ultrastructural Defects in Mitochondrial Myopathy.Semantic proximity Read ↗

Mitofusin 2 Dysfunction and Disease in Mice and MenSemantic proximity Read ↗

Mitochondrial "dysmorphology" in variant classification.Semantic proximity Read ↗

Clinico-Radiological and Genotypic Spectrum of Nuclear Mitochondriopathies.Semantic proximity Read ↗

[Molecular pathogenesis of hereditary motor and sensory neuropathy].Semantic proximity Read ↗

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