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 case of complete form of pachydermoperiostosis with SLCO2A1 mutations.

European journal of dermatology : EJD - 1 Apr 2021

Xu Cui, Tao Yue

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 Adolescent
Share to Heterozygote
Share to Mutation
Share to Organic Anion Transporters

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Radiography

Source

Identifiers

PMID: 34001473
DOI: 10.1684/ejd.2021.4003

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

A case of complete form of pachydermoperiostosis with SLCO2A1 mutations.PMID 34001473Read ↗

Complete form of pachydermoperiostosis with SLCO2A1 gene mutation in a Korean family.Semantic proximity Read ↗

Complete type of pachydermoperiostosis with a novel mutation c.510G>A of the SLCO2A1 gene.Semantic proximity Read ↗

Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations.Semantic proximity Read ↗

The complete type of pachydermoperiostosis: a novel nonsense mutation p.E141* of the SLCO2A1 gene.Semantic proximity Read ↗

The novel SLCO2A1 heterozygous missense mutation p.E427K and nonsense mutation p.R603* in a female patient with pachydermoperiostosis with an atypical phenotype.Semantic proximity Read ↗

Pachydermoperiostosis in an African patient caused by a Chinese/Japanese SLCO2A1 mutation-case report and review of literature.Semantic proximity Read ↗

Complete Form of Pachydermoperiostosis with Good Initial Response to Etoricoxib: A Case ReportSemantic proximity Read ↗

Successful treatment of pachydermoperiostosis with etoricoxib in a patient with a homozygous splice-site mutation in the SLCO2A1 gene.Semantic proximity Read ↗

Chronic Enteropathy Associated with SLCO2A1 with Pachydermoperiostosis.Semantic proximity Read ↗

Complete form of pachydermoperiostosis: a case report.Semantic proximity Read ↗

Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis.Semantic proximity Read ↗

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.Semantic proximity Read ↗

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