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

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

Journal of genetics - 1 Sept 2015

Mehrjoo Zohreh, Babanejad Mojgan, Kahrizi Kimia, Najmabadi Hossein

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 Connexin 26
Share to Connexins
Share to Consanguinity
Share to Deafness

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Recessive

Share to Pakistan

Share to Saudi Arabia

Source

Identifiers

PMID: 26440088
DOI: 10.1007/s12041-015-0537-6

Genes

ILDR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families.PMID 26440088Read ↗

ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population.Semantic proximity Read ↗

Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature.Semantic proximity Read ↗

Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.Semantic proximity Read ↗

A novel LOXHD1 variant in a Chinese couple with hearing loss.Semantic proximity Read ↗

A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.Semantic proximity Read ↗

A Novel Missense Variant in the ESRRB Gene Causing Nonsyndromic Hearing Loss: In Silico Analyses of a CaseSemantic proximity Read ↗

Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.Semantic proximity Read ↗

A Novel p.G141R Mutation in ILDR1 Leads to Recessive Nonsyndromic Deafness DFNB42 in Two Chinese Han Families.Semantic proximity Read ↗

A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case.Semantic proximity Read ↗

Genetic and clinical aspects of TMC1-related hearing loss in Iranian families: identification of two novel variants.Semantic proximity Read ↗

A novel autosomal recessive DEAF1 nonsense variant: expanding the clinical phenotype.Semantic proximity Read ↗

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

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