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1. College of Medicine (의과대학)
Dept. of Laboratory Medicine (진단검사의학교실)
1. Journal Papers
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Showing results 8 to 13 of 13
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Journal Title
2022
In vivo outer hair cell gene editing ameliorates progressive hearing loss in dominant-negative Kcnq4 murine model
THERANOSTICS
2014
Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.
LARYNGOSCOPE
2015
Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene
EXPERIMENTAL AND MOLECULAR MEDICINE
2022
OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin
AUTOPHAGY
2019
Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency
Scientific Reports
2019
The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report
BMC MEDICAL GENETICS
1
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