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 Mutation of PRKAR1A Caused Carney Complex in a Chinese Patient.

Chinese medical journal - 20 Dec 2017

Cai Xiao-Ling, Wu Jing, Luo Ying-Ying, Chen Ling, Han Xue-Yao, Ji Li-Nong

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 Asian People
Share to Carney Complex
Share to Cyclic AMP-Dependent Protein Kinase RIalpha Subunit
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Transcription Factors

Source

Open in PubMed Open full text

Identifiers

PMID: 29237939
DOI: 10.4103/0366-6999.220309
PMCID: PMC5742934

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Novel Mutation of PRKAR1A Caused Carney Complex in a Chinese Patient.PMID 29237939Read ↗

A novel PRKAR1A gene mutation in Carney complex.Semantic proximity Read ↗

A novel PRKAR1A mutation resulting in a splicing variant in a case of Carney complex.Semantic proximity Read ↗

Carney complex: a curious case of a rare cancer syndrome caused by a novel pathogenic mutation in the PRKAR1A gene.Semantic proximity Read ↗

Novel PRKAR1A mutation in Carney complex: a case report and literature review.Semantic proximity Read ↗

A novel splice site mutation of the PRKAR1A gene, C.440+5 G>C, in a Chinese family with Carney complex.Semantic proximity Read ↗

Phenotypic Variability in a Family with Carney Complex Accompanied by a Novel Mutation Involving PRKAR1A.Semantic proximity Read ↗

Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient EvaluationSemantic proximity Read ↗

Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient EvaluationSemantic proximity Read ↗

Association of Carney Complex with an Intronic Splice Site Mutation in the PRKAR1A Gene.Semantic proximity Read ↗

Case studies of two related Chinese patients with Carney complex presenting with extensive cardiac myxomas and PRKAR1A gene mutation of c.491_492delTG.Semantic proximity Read ↗

A Novel Inherited Mutation in PRKAR1A Abrogates PreRNA Splicing in a Carney Complex Family.Semantic proximity Read ↗

Unusual presentations of Carney Complex in patient with a novel PRKAR1A mutation.Semantic proximity Read ↗

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