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

Severe congenital neutropenia: a negative synergistic effect of multiple mutations of ELANE (ELA2) gene.

British journal of haematology - 1 Sept 2009

Lanciotti Marina, Caridi Gianluca, Rosano Camillo, Pigullo Simona, Lanza Tiziana, Dufour Carlo

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 Leukocyte Elastase
Share to Mutation
Share to Neutropenia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Protein Conformation

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 19594744
DOI: 10.1111/j.1365-2141.2009.07787.x

Genes

ELANE

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

Severe congenital neutropenia: a negative synergistic effect of multiple mutations of ELANE (ELA2) gene.PMID 19594744Read ↗

Severe congenital neutropenia with a novel ELANE mutation in 2 Mexican patients.Semantic proximity Read ↗

[Clinical and genetic analysis of two patients with congenital neutropenia caused by ELANE gene mutation].Semantic proximity Read ↗

A novel mutation Ala57Val of the ELA2 gene in a Korean boy with severe congenital neutropenia.Semantic proximity Read ↗

Spectrum of ELANE mutations in congenital neutropenia: a single-centre study in patients of Indian origin.Semantic proximity Read ↗

[Congenital neutropenia caused by ELANE gene mutation: a case report].Semantic proximity Read ↗

Different clinical phenotypes in familial severe congenital neutropenia cases with same mutation of the ELANE gene.Semantic proximity Read ↗

Screening for ELANE, HAX1 and GFI1 gene mutations in children with neutropenia and clinical characterization of two novel mutations in ELANE gene.Semantic proximity Read ↗

[Mutations of the ELANE gene cause severe congenital neutropenia with periodontal disease: a case report].Semantic proximity Read ↗

Identifying Two Novel Mutations and MDS/AML Outcome of Severe Congenital Neutropenia/Cyclic NeutropeniaSemantic proximity Read ↗

Digenic mutations in severe congenital neutropenia.Semantic proximity Read ↗

Pediatric autoimmune diseases with ELANE gene mutation associated with neutropeniaSemantic proximity Read ↗

Genetic insights into congenital neutropenia.Semantic proximity Read ↗

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