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

OBJECTIVES: Hearing 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 sequen...

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Detalles Bibliográficos
Autores principales: Kim, Hee-Jung, Park, Chang-Hun, Kim, Hee-Jin, Lee, Ki-O, Won, Hong-Hee, Ko, Moon-Hee, Chu, Hosuk, Cho, Yang-Sun, Chung, Won-Ho, Kim, Jong-Won, Hong, Sung Hwa
Formato: Texto
Lenguaje:English
Publicado: Korean Society of Otorhinolaryngology-Head and Neck Surgery 2010
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896735/
https://www.ncbi.nlm.nih.gov/pubmed/20607074
http://dx.doi.org/10.3342/ceo.2010.3.2.65

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896735/
https://www.ncbi.nlm.nih.gov/pubmed/20607074
http://dx.doi.org/10.3342/ceo.2010.3.2.65

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