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

Clinical utility gene card for: Nemaline myopathy - update 2015.

European journal of human genetics : EJHG - 1 Nov 2015

Nowak Kristen J, Davis Mark R, Wallgren-Pettersson Carina, Lamont Phillipa J, Laing Nigel 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 Genetic Predisposition to Disease
Share to Genetic Testing
Share to Muscle Proteins
Share to Muscle, Skeletal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Myopathies, Nemaline

Share to Tropomyosin

Source

Open in PubMed Open full text

Identifiers

PMID: 25712079
DOI: 10.1038/ejhg.2015.12
PMCID: PMC4613474

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

Clinical utility gene card for: Nemaline myopathy - update 2015.PMID 25712079Read ↗

Clinical utility gene card for: nemaline myopathy.Semantic proximity Read ↗

Clinical utility gene card for: Meckel syndrome - update 2016.Semantic proximity Read ↗

Clinical utility gene card for: CHARGE syndrome - update 2015.Semantic proximity Read ↗

Clinical utility gene card for: Proximal spinal muscular atrophy (SMA) - update 2015.Semantic proximity Read ↗

Clinical utility gene card for: Alström syndrome.Semantic proximity Read ↗

Clinical utility gene card for: Menkes disease.Semantic proximity Read ↗

Clinical utility gene card for: Joubert syndrome--update 2013.Semantic proximity Read ↗

Clinical utility gene card for: 3-M syndrome - update 2013.Semantic proximity Read ↗

GNE myopathy: new name and new mutation nomenclature.Semantic proximity Read ↗

Clinical utility gene card for: Alport syndrome - update 2014.Semantic proximity Read ↗

Clinical utility gene card for: mucopolysaccharidosis type II.Semantic proximity Read ↗

Clinical utility gene card for: Lesch-Nyhan syndrome--update 2013.Semantic proximity Read ↗

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