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 LOXHD1 variant in a Chinese couple with hearing loss.

The Journal of international medical research - 1 Dec 2019

Zhang Chuan, Hao Shengju, Liu Yali, Zhou Bingbo, Liu Furong, Zheng Lei, Ma Panpan, Liu Qing, Lin Xiaojuan, Yan Yousheng, Zhang Qinghua

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 Base Sequence
Share to Carrier Proteins
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Loss

Share to Heterozygote

Share to Pregnancy

Share to Pregnancy Outcome

Source

Open in PubMed Open full text

Identifiers

PMID: 31709873
DOI: 10.1177/0300060519884197
PMCID: PMC7045666

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel LOXHD1 variant in a Chinese couple with hearing loss.PMID 31709873Read ↗

Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient CohortSemantic proximity Read ↗

Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1.Semantic proximity Read ↗

Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families.Semantic proximity Read ↗

Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families.Semantic proximity Read ↗

Gene4HL: An Integrated Genetic Database for Hearing LossSemantic proximity Read ↗

Recessive LOXHD1 Variants Cause a Milder Prelingual Hearing Loss: Genotype-Phenotype Correlation and Three Additional Patients With Novel VariantsSemantic proximity Read ↗

A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family.Semantic proximity Read ↗

Recessive LOXHD1 variants cause a prelingual down-sloping hearing loss: genotype-phenotype correlation and three additional children with novel variants.Semantic proximity Read ↗

Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients.Semantic proximity Read ↗

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.Semantic proximity Read ↗

Missense Variant in LOXHD1 is Associated With Canine Nonsyndromic Hearing LossSemantic proximity Read ↗

Auditory phenotype of DFNA1.Semantic proximity Read ↗

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