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.

European journal of human genetics : EJHG - 1 Jun 2012

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 Muscle, Skeletal
Share to Mutation
Share to Myopathies, Nemaline

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Open in PubMed Open full text

Identifiers

PMID: 22510848
DOI: 10.1038/ejhg.2012.70
PMCID: PMC3355270

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 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.PMID 22510848Read ↗

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

Clinical utility gene card for: dilated cardiomyopathy (CMD).Semantic proximity Read ↗

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

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

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

Clinical utility gene card for: adrenoleukodystrophy.Semantic proximity Read ↗

Clinical utility gene card for: achromatopsia.Semantic proximity Read ↗

Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.Semantic proximity Read ↗

Clinical utility gene card for: HMSN/HNPP HMSN types 1, 2, 3, 6 (CMT1,2,4, DSN, CHN, GAN, CCFDN, HNA); HNPP.Semantic proximity Read ↗

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