Auto Inflammatory Syndrome with SLC29A3 Mutation.

doi:10.1007/s12098-023-04980-4

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

Auto Inflammatory Syndrome with SLC29A3 Mutation.

Indian journal of pediatrics - 1 Jul 2024

Jain Abhishek, Maheshwari Anu, Mahto Deonath

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 Autoimmune Diseases
Share to Child
Share to Mutation
Share to Nucleoside Transport Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Syndrome

Source

Open in PubMed

Identifiers

PMID: 38114859
DOI: 10.1007/s12098-023-04980-4

Genes

SLC29A3

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

Auto Inflammatory Syndrome with SLC29A3 Mutation.PMID 38114859Read ↗

Genetic culprit of rare autoinflammatory disorder confirmed.Semantic proximity Read ↗

Gene symbol: SLC3A1.Semantic proximity Read ↗

A Case of SLC29A3 Spectrum Disorder-Unresponsive to Multiple Immunomodulatory Therapies.Semantic proximity Read ↗

The hereditary autoinflammatory syndromes.Semantic proximity Read ↗

A case of neonatal-onset autoinflammatory syndrome with a de novo PSMB9 mutation resembling Nakajo-Nishimura syndromeSemantic proximity Read ↗

A novel SLC39A4 gene mutation in the family of an acrodermatitis enteropathica patient with an unusual presentation.Semantic proximity Read ↗

NEMO splice variant causes distinct autoinflammatory syndrome.Semantic proximity Read ↗

Cryopyrin-associated autoinflammatory syndrome: a new mutation.Semantic proximity Read ↗

Case Report: Gitelman syndrome with a suspected MEFV- associated autoinflammatory phenotype: diagnostic challenges in a complex case.Semantic proximity Read ↗

Gene symbol: SLC45A2.Semantic proximity Read ↗

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