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 novel WISP3 mutation in a Chinese patient with progressive pseudorheumatoid dysplasia.

QJM : monthly journal of the Association of Physicians - 8 Jun 2023

Zou Ya-Dan, Yao Hai-Hong, Li Jia-Chen, Zhang Kai, Li Zhan-Guo

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 East Asian People
Share to Joint Diseases
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 36759945
DOI: 10.1093/qjmed/hcad015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel WISP3 mutation in a Chinese patient with progressive pseudorheumatoid dysplasia.PMID 36759945Read ↗

Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia.Semantic proximity Read ↗

A novel compound heterozygous mutation of WISP3 in progressive pseudorheumatoid dysplasia mimicking juvenile idiopathic arthritis.Semantic proximity Read ↗

Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia.Semantic proximity Read ↗

Identification of a mutation in the WISP3 gene in three unrelated families with progressive pseudorheumatoid dysplasia.Semantic proximity Read ↗

WISP3 mutation associated with pseudorheumatoid dysplasia.Semantic proximity Read ↗

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.Semantic proximity Read ↗

Patients with progressive pseudorheumatoid dysplasia: from clinical diagnosis to molecular studies.Semantic proximity Read ↗

Progressive pseudorheumatoid dysplasia with new-found gene mutation of Wntl inducible signaling pathway protein 3.Semantic proximity Read ↗

A homozygous recurring mutation in WISP3 causing progressive pseudorheumatoid arthropathy.Semantic proximity Read ↗

Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia.Semantic proximity Read ↗

Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype-phenotype analysis of 105 patients.Semantic proximity Read ↗

Molecular study of WISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: identification of two novel mutations, and description of a founder effect.Semantic proximity Read ↗

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