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Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss

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Background: Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syn­dromic HL (ARNSHL) is the most common type of hereditary HL. It is extremely heterogeneous and over 70 loci (known as DFNB) have been identified. This study was launched to determine the re...

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Main Authors: MA Tabatabaiefar (Author), F Alasti (Author), M Montazer Zohour (Author), L Shariati (Author), E Farrokhi (Author), DD Farhud (Author), GV Camp (Author), MR Noori-Daloii (Author), M Hashemzadeh Chaleshtori (Author)
Format: Book
Published: Tehran University of Medical Sciences, 2011-06-01T00:00:00Z.
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3rd Floor Main Library

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