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

Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance

30 Nov 2018

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 Cardiac electrophysiology and arrhythmias
Share to Cardiomyopathy and Myosin Studies
Share to Congenital heart defects research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30498240
DOI: 10.1038/s10038-018-0542-8

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

Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significancePMID 30498240Read ↗

CACNA1C-Related Channelopathies.Semantic proximity Read ↗

Novel heterozygous mutation of CACNA2D1 gene in a Chinese family with arrhythmia.Semantic proximity Read ↗

PharmGKB summary: very important pharmacogene information for CACNA1S.Semantic proximity Read ↗

Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness.Semantic proximity Read ↗

Expanding the phenotype of CACNA1C mutation disorders.Semantic proximity Read ↗

Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young.Semantic proximity Read ↗

Timothy Syndrome and CACNA1C-Related Disorder: First International Language and Management Guidelines Consensus StatementSemantic proximity Read ↗

Clinical Spectrum Of CACNA1C Variants, RevisitedSemantic proximity Read ↗

V876E mutation in CACNA1S gene associated with severe hypokalemic periodic paralysis in a Chinese woman.Semantic proximity Read ↗

CACNA1C (CaV1.2) and other L-type calcium channels in the pathophysiology and treatment of psychiatric disorders: Advances from functional genomics and pharmacoepidemiologySemantic proximity Read ↗

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.Semantic proximity Read ↗

Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.Semantic proximity Read ↗

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