Muscle channelopathies.

doi:10.1016/j.ncl.2014.04.002

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

Back to search

Article

Muscle channelopathies.

Neurologic clinics - 1 Aug 2014

Statland Jeffrey, Phillips Lauren, Trivedi Jaya R

Abstract excerpt

Skeletal muscle channelopathies are rare heterogeneous diseases with marked genotypic and phenotypic variability. Despite advances in understanding of the molecular pathology of these disorders, the diverse phenotypic manifestations remain a challenge in diagnosis and therapeutics. These disorders can cause lifetime disability and affect quality of life. There is no treatment of these disorders approved by the US...

Topics

Channelopathies
Humans
Ion Channels
Muscle, Skeletal
Mutation
Myasthenic Syndromes, Congenital
Myotonia
Myotonic Disorders

Source

Open in PubMed

Identifiers

PMID: 25037091
DOI: 10.1016/j.ncl.2014.04.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics