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

Targeted exome sequencing identified two novel truncation mutations in GPR98 causing Usher syndrome.

Clinical & experimental ophthalmology - 1 Apr 2016

Yang Ji, Huang Xiu-Feng, Tong Yi, Jin Zi-Bing

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 DNA Mutational Analysis
Share to Exome
Share to Pedigree
Share to Receptors, G-Protein-Coupled

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sequence Analysis, DNA

Share to Tomography, Optical Coherence

Share to Usher Syndromes

Share to Young Adult

Source

Identifiers

PMID: 26432996
DOI: 10.1111/ceo.12664

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

Targeted exome sequencing identified two novel truncation mutations in GPR98 causing Usher syndrome.PMID 26432996Read ↗

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.Semantic proximity Read ↗

GPR98 mutations cause Usher syndrome type 2 in males.Semantic proximity Read ↗

A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.Semantic proximity Read ↗

Non-USH2A mutations in USH2 patients.Semantic proximity Read ↗

The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.Semantic proximity Read ↗

USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms.Semantic proximity Read ↗

High-throughput phenotyping of heteromeric human ether-à-go-go-related gene potassium channel variants can discriminate pathogenic from rare benign variantsSemantic proximity Read ↗

Insights from exome sequencing for endocrine disordersSemantic proximity Read ↗

Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency.Semantic proximity Read ↗

G protein-coupled receptors GPR4 and TDAG8 are oncogenic and overexpressed in human cancersSemantic proximity Read ↗

Identification of two novel pathogenic compound heterozygous MYO7A mutations in Usher syndrome by whole exome sequencing.Semantic proximity Read ↗

Response from Original Authors - RE: Six novel rare nonsynonymous mutations for migraine without aura identified by exome sequencing.Semantic proximity Read ↗

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