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

First Report of an SH2D1A Mutation Associated with X-Linked Lymphoproliferative Disease in Turkey

Turkish journal of haematology : official journal of Turkish Society of Haematology - 3 Aug 2018

Kesici Selman, Yılmaz Keskin Ebru, Chiang Samuel C.C., Kasapkara Çiğdem Seher, Sekine Takuya, Akçaboy Meltem, Fettah Ali, Bryceson Yenan T.

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 Biomarkers
Share to Combined Modality Therapy
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fatal Outcome

Share to Genetic Association Studies

Share to Lymphoproliferative Disorders

Share to Signaling Lymphocytic Activation Molecule Associated Protein

Share to Turkey

Source

Open in PubMed Open full text

Identifiers

PMID: 29391328
DOI: 10.4274/tjh.2017.0445
PMCID: PMC6110441

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

First Report of an SH2D1A Mutation Associated with X-Linked Lymphoproliferative Disease in TurkeyPMID 29391328Read ↗

X-linked lymphoproliferative disease with a novel SH2D1A gene mutation.Semantic proximity Read ↗

A novel pathogenic SH2D1A mutation for X-linked lymphoproliferative syndrome type 1.Semantic proximity Read ↗

Study of SH2D1A gene mutation in paediatric patients with B-cell lymphoma.Semantic proximity Read ↗

Novel Mutations in SH2D1A Gene in X-linked Lymphoproliferative Syndrome, Diagnosed After B-Cell Non-Hodgkin Lymphoma.Semantic proximity Read ↗

Potential pathogenic mechanism of type 1 X-linked lymphoproliferative syndrome caused by a mutation of SH2D1A gene in an infant: A case report.Semantic proximity Read ↗

[Two families of X-linked lymphoproliferative disease type 1 characterized by agammaglobulinemia].Semantic proximity Read ↗

Identification of a novel nonsense mutation in SH2D1A in a patient with X-linked lymphoproliferative syndrome type 1: a case report.Semantic proximity Read ↗

X-linked lymphoproliferative disease type 1: a clinical and genetic updateSemantic proximity Read ↗

Variable clinical phenotypes of X-linked lymphoproliferative syndrome in China: Report of five cases with three novel mutations and review of the literature.Semantic proximity Read ↗

A new SH2D1A mutation in a female adult XLP disease with hemophagocytic lymphohistiocytosis and NK-cell leukemia.Semantic proximity Read ↗

A spectrum of mutations in SH2D1A that causes X-linked lymphoproliferative disease and other Epstein-Barr virus-associated illnesses.Semantic proximity Read ↗

The abnormal gene in X-linked lymphoproliferative syndrome.Semantic proximity Read ↗

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