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Annals of Clinical and Laboratory Science|October 16, 2010
Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing lossBorum Sagong, Raekil Park, Yee Hyuk Kim, et al.
Cell Death & Disease|August 3, 2018
Evaluating protective and therapeutic effects of alpha-lipoic acid on cisplatin-induced ototoxicityKyung-Hee Kim, Byeonghyeon Lee, Ye-Ri Kim, et al.
Gene|June 26, 2017
Identification of a novel splicing mutation within SLC17A8 in a Korean family with hearing loss by whole-exome sequencingNari Ryu, Seokwon Lee, Hong-Joon Park, et al.
Human Mutation|April 30, 2019
Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing lossByeonghyeon Lee, Ye-Ri Kim, Sang-Joo Kim, et al.
BMC Medical Genetics|October 29, 2008
Significant association of SREBP-2 genetic polymorphisms with avascular necrosis in the Korean populationTae-Ho Kim, Jeong-In Baek, Jung Min Hong, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine|July 4, 2018
Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapyNari Ryu, Min-A Kim, Dongsik Park, et al.
Biochimica Et Biophysica Acta|September 14, 2010
Pathogenic effects of a novel mutation (c.664_681del) in KCNQ4 channels associated with auditory pathologyJeong-In Baek, Hong-Joon Park, Kyungjoon Park, et al.
Gene|July 10, 2016
Genetic association of MYH genes with hereditary hearing loss in KoreaSang-Joo Kim, Seokwon Lee, Hong-Joon Park, et al.
Human Mutation|September 19, 2014
Identification of pathogenic mechanisms of COCH mutations, abolished cochlin secretion, and intracellular aggregate formation: genotype-phenotype correlations in DFNA9 deafness and vestibular disorderSeung-Hyun Bae, Nahid G Robertson, Hyun-Ju Cho, et al.
Gene|April 9, 2013
Genetic analysis of auditory neuropathy spectrum disorder in the Korean populationSeung-Hyun Bae, Jeong-In Baek, Jong Dae Lee, et al.
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