Log in to save to my catalogue

Loss of MEF2C function by enhancer mutation leads to neuronal mitochondria dysfunction and motor def...

Loss of MEF2C function by enhancer mutation leads to neuronal mitochondria dysfunction and motor def...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5dcd6fb38273477e8a9538fac4c6aa10

Loss of MEF2C function by enhancer mutation leads to neuronal mitochondria dysfunction and motor deficits in mice

About this item

Full title

Loss of MEF2C function by enhancer mutation leads to neuronal mitochondria dysfunction and motor deficits in mice

Publisher

England: BioMed Central Ltd

Journal title

Molecular neurodegeneration, 2025-02, Vol.20 (1), p.16-18

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the loss of both upper and lower motor neurons, leading to progressive paralysis. Both genetic alterations and epigenetic modifications contribute to neuronal dysfunction in the pathogenesis of ALS. However, the mechanism behind genetic mutations in the non-c...

Alternative Titles

Full title

Loss of MEF2C function by enhancer mutation leads to neuronal mitochondria dysfunction and motor deficits in mice

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_5dcd6fb38273477e8a9538fac4c6aa10

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5dcd6fb38273477e8a9538fac4c6aa10

Other Identifiers

ISSN

1750-1326

E-ISSN

1750-1326

DOI

10.1186/s13024-024-00792-y

How to access this item