caa a22 4500 397575610 CHVBK 20180308164855.0 cr unu---uuuuu 161202e199606 xx s 000 0 eng 10.1093/hmg/5.6.849 doi (NATIONALLICENCE)oxford-10.1093/hmg/5.6.849 A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness (DFNA11) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene [Elektronische Daten] [Yuya Tamagawa, Ken Kitamura, Takashi Ishida, Kazuhiro Ishikawa, Hajime Tanaka, Shoji Tsuji, Masatoyo Nishizawa] Hereditary hearing loss is divided into two groups, syndromic and non-syndromic, the latter being more common and highly heterogeneous. Linkage analyses were performed on a Japanese family showing a dominant form of non-syndromic progressive sensori-neural hearing loss. This gene (DFNA11) was localized within the region of chromosome 11q which contains the second gene for a recessive form of non-syndromic sensorineural hearing loss (DFNB2). Since it has been reported that another gene for dominant non-syndromic hearing loss (DFNA3) has been mapped to the same region as the first gene for recessive hearing loss (DFNB1), it is possible that different mutations in the DFNB2 gene may result in either dominant or recessive hearing loss. © 1996 Oxford University Press Tamagawa Yuya Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut Kitamura Ken Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut Ishida Takashi Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut Ishikawa Kazuhiro Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut Tanaka Hajime Department of Neurology, Brain Research Institute, Niigata University, Asahimachi, Niigata 951, Japan aut Tsuji Shoji Department of Neurology, Brain Research Institute, Niigata University, Asahimachi, Niigata 951, Japan aut Nishizawa Masatoyo Department Neurology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut Human Molecular Genetics Oxford University Press 5/6(1996-06), 849-852 0964-6906 5:6<849 1996 5 hmg https://doi.org/10.1093/hmg/5.6.849 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1093/hmg/5.6.849 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Tamagawa Yuya Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut NATIONALLICENCE 700 1- Kitamura Ken Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut NATIONALLICENCE 700 1- Ishida Takashi Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut NATIONALLICENCE 700 1- Ishikawa Kazuhiro Department of Otolaryngology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut NATIONALLICENCE 700 1- Tanaka Hajime Department of Neurology, Brain Research Institute, Niigata University, Asahimachi, Niigata 951, Japan aut NATIONALLICENCE 700 1- Tsuji Shoji Department of Neurology, Brain Research Institute, Niigata University, Asahimachi, Niigata 951, Japan aut NATIONALLICENCE 700 1- Nishizawa Masatoyo Department Neurology, Jichi Medical School, Minamikawachi, Tochigi 329-04, Japan aut NATIONALLICENCE 773 0- Human Molecular Genetics Oxford University Press 5/6(1996-06), 849-852 0964-6906 5:6<849 1996 5 hmg Metadata rights reserved CC BY-NC-4.0 http://creativecommons.org/licenses/by-nc/4.0 nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-oxford