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

A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.

Annals of hematology - 1 Feb 2011

Gundel Florian, Eber Stefan, Heep Axel

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 Ankyrins
Share to Exons
Share to Infant, Newborn
Share to Infant, Newborn, Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Spherocytosis, Hereditary

Source

Identifiers

PMID: 20512576
DOI: 10.1007/s00277-010-0989-y

Genes

ANK1

Variants

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

A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.PMID 20512576Read ↗

Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis.Semantic proximity Read ↗

Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis.Semantic proximity Read ↗

[Identification of a novel ANK1 gene mutation in a newborn with hereditary spherocytosis].Semantic proximity Read ↗

A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis.Semantic proximity Read ↗

A de novo ANK1 mutation associated to hereditary spherocytosis: a case reportSemantic proximity Read ↗

A Novel de novo Mutation in ANK1 Gene Identified through Targeted Next-Generation Sequencing in a Neonate with Hereditary Spherocytosis.Semantic proximity Read ↗

Clinical manifestations and phenotypic analysis of new ANK1 gene mutations in 12 Chinese children with hereditary spherocytosisSemantic proximity Read ↗

A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report.Semantic proximity Read ↗

Novel hereditary spherocytosis-associated splice site mutation in the ANK1 gene caused by parental gonosomal mosaicism.Semantic proximity Read ↗

Hematologically important mutations: ankyrin variants in hereditary spherocytosis.Semantic proximity Read ↗

Identification of a novel ANK1 c.856C>T nonsense mutation in two patients from a Chinese family with hereditary spherocytosis by NGSSemantic proximity Read ↗

Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.Semantic proximity Read ↗

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