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 Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis.

Genes - 10 Jan 2021

An Joon-Yong, Jung Jae Ho, Choi Leejee, Wieben Eric D, Mohney Brian G

Abstract excerpt

PURPOSE: To investigate candidate genes associated with familial strabismus and propose a theory of their interaction in familial strabismus associated with early neurodevelopment. METHODS: Eighteen families, including 53 patients diagnosed with strabismus and 34 unaffected family members, were analyzed. All patients with strabismus and available unaffected family members were evaluated using whole exome...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cadherins
Share to Case-Control Studies
Share to Epidermal Growth Factor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to ERG1 Potassium Channel

Share to Exome Sequencing

Share to Genetic Testing

Share to Membrane Proteins

Share to Strabismus

Source

Open in PubMed Open full text

Identifiers

PMID: 33435129
DOI: 10.3390/genes12010075
PMCID: PMC7827096

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

Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis.PMID 33435129Read ↗

Genome-Wide Association Study and Rare Variant Association Studies of Strabismus in the All of Us Research ProgramSemantic proximity Read ↗

Identification of 2 Potentially Relevant Gene Mutations Involved in Strabismus Using Whole-Exome Sequencing.Semantic proximity Read ↗

Genetics of strabismusSemantic proximity Read ↗

Identification of rare paired box 3 variant in strabismus by whole exome sequencingSemantic proximity Read ↗

An Update on the Genetics of Comitant StrabismusSemantic proximity Read ↗

Strabismus genetics across a spectrum of eye misalignment disordersSemantic proximity Read ↗

A commonly occurring genetic variant within the NPLOC4–TSPAN10–PDE6G gene cluster is associated with the risk of strabismusSemantic proximity Read ↗

Risk Factors and Genetics in Common Comitant StrabismusSemantic proximity Read ↗

Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome regionSemantic proximity Read ↗

Missense mutation in the PAX6 gene can cause a complex mild variable phenotype predominated by concomitant strabismus.Semantic proximity Read ↗

Genomic Copy Number Variants Associated With Strabismus and Amblyopia in the All of Us Research Program.Semantic proximity Read ↗

The Genetic Basis of Incomitant Strabismus: Consolidation of the Current Knowledge of the Genetic Foundations of DiseaseSemantic proximity Read ↗

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