A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct

por Sagong, Borum, Baek, Jeong-In, Lee, Kyu-Yup, Kim, Un-Kyung
Publicado 2017

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

por Woo, Hae-Mi, Park, Hong-Joon, Baek, Jeong-In, Park, Mi-Hyun, Kim, Un-Kyung, Sagong, Borum, Koo, Soo Kyung
Publicado 2013

Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans

por Ryu, Nari, Sagong, Borum, Park, Hong-Joon, Kim, Min-A, Lee, Kyu-Yup, Choi, Jae Young, Kim, Un-Kyung
Publicado 2016

Evaluation of the Contribution of the EYA4 and GRHL2 Genes in Korean Patients with Autosomal Dominant Non-Syndromic Hearing Loss

por Kim, Ye-Ri, Kim, Min-A, Sagong, Borum, Bae, Seung-Hyun, Lee, Hyo-Jeong, Kim, Hyung-Jong, Choi, Jae Young, Lee, Kyu-Yup, Kim, Un-Kyung
Publicado 2015

Genetic Analysis of Genes Related to Tight Junction Function in the Korean Population with Non-Syndromic Hearing Loss

por Kim, Min-A, Kim, Ye-Ri, Sagong, Borum, Cho, Hyun-Ju, Bae, Jae Woong, Kim, Jeongho, Lee, Jinwook, Park, Hong-Joon, Choi, Jae Young, Lee, Kyu-Yup, Kim, Un-Kyung
Publicado 2014

A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population

por Sagong, Borum, Baek, Jeong-In, Oh, Se-Kyung, Na, Kyung Jin, Bae, Jae Woong, Choi, Soo Young, Jeong, Ji Yun, Choi, Jae Young, Lee, Sang-Heun, Lee, Kyu-Yup, Kim, Un-Kyung
Publicado 2013