A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population - Imtiaz, Faiqa; Taibah, Khalid; Ramzan, Khushnooda; Bin-Khamis, Ghada; Kennedy, Shelley; Al-Mubarak, Bashayer; Trabzuni, Daniah; Allam, Rabab; Al-Mostafa, Abeer; Sogaty, Sameera; Al-Shaikh, Abdulmoneem H; Bamukhayyar, Saeed S; et al. (BMC medical genetics, 2011)
Keywords: Analysis; Biomedical and Life Sciences; Biomedicine; Clinical-Molecular Genetics and Cytogenetics; Connexin 26; Connexins - genetics; Cytogenetics; Demographic aspects; Family; Gene Function; Genes, Recessive; Genetic aspects; Genetic Heterogeneity; Genetic Linkage; Genetic susceptibility; Genetic Testing; Hearing loss; Hearing Loss - epidemiology; Hearing Loss - genetics; Human Genetics; Humans; Medical screening; Methods; Mutation; Research Article; Risk factors; Saudi Arabia - epidemiology; Saudi Arabia; Unaffected Sibling; GJB6 Gene; Homozygosity Mapping; Multipoint Linkage Analysis; Hearing Loss