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NTIS 바로가기Clinical and experimental otorhinolaryngology, v.3 no.2, 2010년, pp.65 - 69
Kim, Hee-Jung (Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) , Park, Chang-Hun (Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) , Kim, Hee-Jin (Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) , Lee, Ki-O (Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Korea.) , Won, Hong-Hee (Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Korea.) , Ko, Moon-Hee (Department of Otorhinolaryngology and Head & Neck Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) , Chu, Hosuk (Department of Otorhinolaryngology and Head & Neck Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) , Cho, Yang-Sun (Department of Otorhinolaryngology and Head & Neck Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) , Chung, Won-Ho (Department of Otorhinol) , Kim, Jong-Won , Hong, Sung Hwa
ObjectivesHearing impairment (HI) is the most common sensory deficit in human. The Gap Junction Protein, Beta-2 (GJB2) gene encodes the protein connexin 26, and this gene accounts for up to half of the cases of autosomal recessive nonsyndromic HI. This study was conducted to obtain a set of sequence...
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