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A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9

A second kindred has been identified which supports the previously reported location of DFNB9. Linkage has been established to markers closely linked to DFNB9 which is located on 2p22-p23. The hearing impaired individuals in this highly consanguineous kindred from Eastern Turkey have prelingual prof...

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Detaylı Bibliyografya
Yayımlandı:Eur J Hum Genet
Asıl Yazarlar: Leal, Suzanne M, Apaydin, Fazil, Barnwell, Carol, Iber, Metin, Kandogan, Tolga, Pfister, Markus, Braendle, Uwe, Cura, Orhan, Schwalb, Marvin, Zenner, Hans-Peter, Vitale, Emilia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1998
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6141006/
https://ncbi.nlm.nih.gov/pubmed/9781041
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5200201
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