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

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

<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...

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Main Authors: Al-Shaikh Abdulmoneem H (Author), Sogaty Sameera (Author), Al-Mostafa Abeer (Author), Allam Rabab (Author), Trabzuni Daniah (Author), Al-Mubarak Bashayer (Author), Kennedy Shelley (Author), Bin-Khamis Ghada (Author), Ramzan Khushnooda (Author), Taibah Khalid (Author), Imtiaz Faiqa (Author), Bamukhayyar Saeed S (Author), Meyer Brian F (Author), Al-Owain Mohammed (Author)
Format: Book
Published: BMC, 2011-07-01T00:00:00Z.
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3rd Floor Main Library

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