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

EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome.

Journal of neurology - 1 Jul 2016

Gargaun Elena, Seferian Andreea Mihaela, Cardas Ruxandra, Le Moing Anne-Gaelle, Delanoe Catherine, Nectoux Juliette, Nelson Isabelle, Bonne Gisèle, Bihoreau Marie-Thérèse, Deleuze Jean-François, Boland Anne, Masson Cécile, Servais Laurent, Gidaro Teresa

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 Child, Preschool
Share to DNA Mutational Analysis
Share to Early Growth Response Protein 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to EGR2 gene

Share to Hereditary Sensory and Motor Neuropathy

Share to Mutation

Source

Identifiers

PMID: 27159987
DOI: 10.1007/s00415-016-8153-9

Genes

EGR2

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

EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome.PMID 27159987Read ↗

Major review: Exfoliation syndrome; advances in disease genetics, molecular biology, and epidemiologySemantic proximity Read ↗

Update of Emerinopathies’ clinical-genetic spectrum: the French network experienceSemantic proximity Read ↗

EEC syndrome-like phenotype in a patient with an IRF6 mutation.Semantic proximity Read ↗

MEGDEL Syndrome: Expanding the Phenotype and New Mutations.Semantic proximity Read ↗

Clinical Spectrum of PRKAG2 Syndrome.Semantic proximity Read ↗

[Muenke syndrome].Semantic proximity Read ↗

US case of the day. Pena-Shokeir phenotype.Semantic proximity Read ↗

Non-lethal non-mosaic male with Conradi-Hunermann syndrome caused by a novel EBP c.356T>G mutation.Semantic proximity Read ↗

[Ekbom syndrome].Semantic proximity Read ↗

Alport syndrome--clinical phenotypes, incidence, and pathology.Semantic proximity Read ↗

Clinical phenotypes of MAGEL2 mutations and deletions.Semantic proximity Read ↗

[SHOX haploinsufficiency].Semantic proximity Read ↗

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