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• W1567220042 abstract "Hearing loss (HL) is the most common sensory defect in human beings, affecting 1.86 in 1000 newborns around the world which half of it is due to genetic causes (Morton & Nance, 2006). HL can be syndromic or nonsyndromic. Individuals affected with syndromic form have additional clinical signs whereas nonsyndromic HL is not associated with other clinical signs and symptoms. All Mendelian pattern of inheritance have been observed in nonsyndromic HL (NSHL) including autosomal dominant (AD), autosomal recessive (AR), X-linked inheritance (XL) and mitochondrial inheritance (MT); autosomal recessive is the main form of NSHL, i.e. 75-85 % of NSHL show AR pattern in affected pedigrees." @default.
• W1567220042 created "2016-06-24" @default.
• W1567220042 creator A5003607219 @default.
• W1567220042 creator A5011503775 @default.
• W1567220042 creator A5059023161 @default.
• W1567220042 date "2012-03-28" @default.
• W1567220042 modified "2023-10-04" @default.
• W1567220042 title "Genetics of Hearing Loss" @default.
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