Persistent Unexplained Transaminitis in COPA Syndrome.

doi:10.1007/s10875-020-00832-4

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

Persistent Unexplained Transaminitis in COPA Syndrome.

Journal of clinical immunology - 1 Jan 2021

Thaivalappil Silpa S, Garrod Andrea S, Borowitz Stephen M, Watkin Levi B, Lawrence Monica G

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 DNA Mutational Analysis
Share to Immune System Diseases
Share to Immunohistochemistry

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Lung

Share to Syndrome

Share to Tomography, X-Ray Computed

Share to Transaminases

Source

Open in PubMed

Identifiers

PMID: 32970305
DOI: 10.1007/s10875-020-00832-4

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 · 8 closest

Persistent Unexplained Transaminitis in COPA Syndrome.PMID 32970305Read ↗

What is causing transaminitis in this 25-year-old patient?Semantic proximity Read ↗

TAP deficiency syndrome.Semantic proximity Read ↗

[A pathogenic mutation in the COPA gene causes a family of COPA syndrome].Semantic proximity Read ↗

First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation.Semantic proximity Read ↗

Functional Validation of a COPA Mutation Broadens the Spectrum of COPA Syndrome.Semantic proximity Read ↗

What syndrome is this? Cockayne syndrome.Semantic proximity Read ↗

Clinical utility gene card for: Trimethylaminuria - update 2014.Semantic proximity Read ↗

[C9 deficiency].Semantic proximity Read ↗

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