Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.

doi:10.3390/genes12040566

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Article

Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.

Genes - 13 Apr 2021

Santos-Cortez Regie Lyn P, Yarza Talitha Karisse L, Bootpetch Tori C, Tantoco Ma Leah C, Mohlke Karen L, Cruz Teresa Luisa G, Chiong Perez Mary Ellen, Chan Abner L, Lee Nanette R, Tobias-Grasso Celina Ann M, Reyes-Quintos Maria Rina T, Cutiongco-de la Paz Eva Maria, Chiong Charlotte M

Abstract excerpt

Background: Hearing loss remains an important global health problem that is potentially addressed through early identification of a genetic etiology, which helps to predict outcomes of hearing rehabilitation such as cochlear implantation and also to mitigate the long-term effects of comorbidities. The identification of variants for hearing loss and detailed descriptions of clinical phenotypes in patients from...

Topics

Child
Child, Preschool
Cochlear Implantation
Female
Gene Regulatory Networks
Genetic Predisposition to Disease
Genetic Variation
Hearing Loss
Humans

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Male

Myosins

Nerve Tissue Proteins

Oncogene Proteins

Phenotype

Phosphoric Diester Hydrolases

Temporal Bone

Tumor Suppressor Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 33924653
DOI: 10.3390/genes12040566
PMCID: PMC8069784

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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