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Article

Identification of novel CDH23 variants linked to hearing loss in a Chinese family: A case report.

Medicine - 13 Sept 2024

Sun Jing, Ren Dawei, Gong Meiheng, Guo Xinyi, Zhang Yan, Du Bo

Abstract excerpt

RATIONALE: Deafness is associated with both environmental and genetic factors, with hereditary deafness often caused by mutations in deafness-related genes. Identifying and analyzing deafness-related genes will aid in early diagnosis and pave the way for treating inherited deafness through gene therapy in the future. PATIENT CONCERNS: A 15-month-old girl underwent audiological examination at the outpatient clinic...

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Share to Cadherin Related Proteins
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 39287240
DOI: 10.1097/MD.0000000000039360
PMCID: PMC11404951

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Identification of novel CDH23 variants linked to hearing loss in a Chinese family: A case report.PMID 39287240Read ↗

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