@article{e978b60111694e22a7de9283aac194c6,
title = "The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population",
keywords = "Connexin26, Connexin30, Deafness, Gap junctions, GJB2, GJB6, Hearing impairment",
author = "Asli Sirmaci and Duygu Akcayoz-Duman and Mustafa Tekin",
note = "Funding Information: The authors are grateful to Dr Ignacio Del-Castillo from the Unidad de Genetica Molecular, Hospital Ramon y Cajal, Madrid, Spain, and to Dr Arti Pandya from the Department of Human Genetics, Virginia Commonwealth University, Richmond, VA, USA, for providing positive control DNA samples. This study was supported by the Turkish Academy of Sciences in the frame-work of the young scientist award program (contract grant number: MT/TUBA-GEBIP/2001-2-19) and Ankara University Scientific Research Projects Department. Copyright: Copyright 2009 Elsevier B.V., All rights reserved.",
year = "2006",
month = dec,
doi = "10.1007/BF02935334",
language = "English (US)",
volume = "85",
pages = "213--216",
journal = "Journal of Genetics",
issn = "0022-1333",
publisher = "Springer India",
number = "3",
}