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

Congenital myasthenic syndromes:gene mutations.

Neuromuscular disorders : NMD - 1 Dec 2003

Ohno Kinji, Engel Andrew G

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 Chromosome Mapping
Share to Mutation
Share to Myasthenic Syndromes, Congenital

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14719537
DOI: 10.1016/s0960-8966(03)00210-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital myasthenic syndromes:gene mutations.PMID 14719537Read ↗

Congenital myasthenic syndromes: gene mutations.Semantic proximity Read ↗

Congenital myasthenic syndromes: gene mutations.Semantic proximity Read ↗

Congenital myasthenic syndromes: gene mutations.Semantic proximity Read ↗

Congenital myasthenic syndromes: gene mutations.Semantic proximity Read ↗

Congenital myasthenic syndromes: gene mutation.Semantic proximity Read ↗

Congenital myasthenic syndromes: gene mutation.Semantic proximity Read ↗

Congenital myasthenic syndromes.Semantic proximity Read ↗

Congenital myasthenic syndromes.Semantic proximity Read ↗

Congenital myasthenic syndromes.Semantic proximity Read ↗

Congenital Myasthenic Syndromes.Semantic proximity Read ↗

Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity.Semantic proximity Read ↗

The Increasing Genetic and Phenotypical Diversity of Congenital Myasthenic Syndromes.Semantic proximity Read ↗

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