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Showing results 1 to 4 of 4

1
A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation

Chung, Juyong; Park, Sang Min; Chang, Sun O.; Chung, Taesu; Lee, Kyoung Yeul; Kim, Ah Reum; Park, Joo Hyun; et al, JOURNAL OF MOLECULAR MEDICINE-JMM, v.92, no.6, pp.651 - 663, 2014-06

2
Destabilization and Mislocalization of POU3F4 by C-Terminal Frameshift Truncation and Extension Mutation

Choi, Byung Yoon; Kim, Do-Hwan; Chung, Taesu; Chang, Mi; Kim, Eun-Hye; Kim, Ah Reum; Seok, Jungirl; et al, HUMAN MUTATION, v.34, no.2, pp.309 - 316, 2013-02

3
Downsloping High-Frequency Hearing Loss Due to Inner Ear Tricellular Tight Junction Disruption by a Novel ILDR1 Mutation in the Ig-Like Domain

Kim, Nayoung K. D.; Higashi, Tomohito; Lee, Kyoung Yeul; Kim, Ah Reum; Kitajiri, Shin-ichiro; Kim, Min Young; Chang, Mun Young; et al, PLOS ONE, v.10, no.2, 2015-02

4
Identification and Clinical Implications of Novel MY015A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing

Chang, Mun Young; Kim, Ah Reum; Kim, Nayoung K. D.; Lee, Chung; Lee, Kyoung Yeul; Jeon, Woo-Sung; Koo, Ja-Won; et al, MOLECULES AND CELLS, v.38, no.9, pp.781 - 788, 2015-09

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