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Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea 원문보기

Clinical 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

Abstract AI-Helper 아이콘AI-Helper

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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참고문헌 (20)

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