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Autosomal recessive nonsyndromic deafness genes: a review

More than 50 percent of prelingual hearing loss is genetic in origin, and of these up to 93 percent are monogenic autosomal recessive traits. Some forms of genetic deafness can be recognized by their associated syndromic features, but in most cases, hearing loss is the only finding and is referred t...

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Bibliografische gegevens
Hoofdauteurs: Duman, Duygu, Tekin, Mustafa
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2012
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3683827/
https://ncbi.nlm.nih.gov/pubmed/22652773
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