Sun Y. Joo
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 32 publications
Auditory genotype-phenotype correlation of patients with variants in STRC.
Journal: Scientific reports
Published: July 15, 2025
The audiological phenotype of patients with a variant in MYH9 and MYH14 genes.
Journal: Scientific reports
Published: April 18, 2025
Antisense oligonucleotide therapy mitigates autosomal dominant progressive hearing loss in a murine model of human DFNA2.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: January 21, 2025
Gene supplementation with precise transgene expression rescues hearing loss in a mouse model with an Mpzl2 East Asian founder variant.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: December 02, 2024
Biallelic variants of SEMA3F are associated with nonsyndromic hearing loss.
Journal: Molecules and cells
Published: September 24, 2024
MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss.
Journal: Experimental & molecular medicine
Published: March 04, 2024
Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss.
Journal: Journal of clinical medicine
Published: February 27, 2024
Evaluation of clinical factors predicting dysphagia in patients with traumatic and non-traumatic cervical spinal cord injury: a retrospective study.
Journal: Frontiers in neurology
Published: January 25, 2024
Novel Variant in CEP250 Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss.
Journal: Cells
Published: July 25, 2023
Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.
Journal: Journal of Korean medical science
Published: June 15, 2023
Last Updated: 09/26/2026