[Unusual phenotype of myopathy associated with a new PNPLA2 mutation].

doi:10.1051/medsci/201632s203

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

Community

Back to search

Article

[Unusual phenotype of myopathy associated with a new PNPLA2 mutation].

Medecine sciences : M/S - 1 Nov 2016

Jousserand Guillemette, Streichenberger Nathalie, Petiot Philippe

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 Biopsy
Share to Cardiomyopathies
Share to Lipase
Share to Lipid Metabolism, Inborn Errors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lipids

Share to Muscle Cells

Share to Muscular Diseases

Share to Muscular Dystrophies

Source

Open in PubMed

Identifiers

PMID: 27869069
DOI: 10.1051/medsci/201632s203

Genes

PNPLA2

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

[Unusual phenotype of myopathy associated with a new PNPLA2 mutation].PMID 27869069Read ↗

Familial polyglucosan body myopathy with unusual phenotype.Semantic proximity Read ↗

[A new type of myotonic dystrophy].Semantic proximity Read ↗

[Congenital and other myopathies].Semantic proximity Read ↗

[Phenotypic heterogeneity of Duchenne myopathy and prognosis criteria].Semantic proximity Read ↗

A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation.Semantic proximity Read ↗

[Duchenne's myopathy in the era of molecular biology].Semantic proximity Read ↗

A myopathy with unusual features caused by PNPLA2 gene mutations.Semantic proximity Read ↗

[X-linked myotubular myopathy].Semantic proximity Read ↗

Novel TTN Mutation Causing Congenital Myopathy.Semantic proximity Read ↗

[A new type of periodic paralysis: Andersen-Tawil syndrome].Semantic proximity Read ↗

[Bethlem myopathy: when the phenotype is misleading].Semantic proximity Read ↗

[Congenital mild nemaline myopathy].Semantic proximity Read ↗

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