A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

• Asıl Yazarlar: Al-Shaikh Abdulmoneem H (Yazar), Sogaty Sameera (Yazar), Al-Mostafa Abeer (Yazar), Allam Rabab (Yazar), Trabzuni Daniah (Yazar), Al-Mubarak Bashayer (Yazar), Kennedy Shelley (Yazar), Bin-Khamis Ghada (Yazar), Ramzan Khushnooda (Yazar), Taibah Khalid (Yazar), Imtiaz Faiqa (Yazar), Bamukhayyar Saeed S (Yazar), Meyer Brian F (Yazar), Al-Owain Mohammed (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: BMC, 2011-07-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Hearing loss is a clinically and genetically heterogeneous disorder. Mutations in the <it>DFNB1 </it>locus have been reported to be the most common cause of autosomal recessive non-syndromic hearing loss worldwide. Apart...