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The most common phenotypes of sensitization to inhalant allergens in childhood

✍ Scribed by K. STORM VAN'S GRAVESANDE; M. MOSELER; J. KUEHR

Book ID
108686991
Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
544 KB
Volume
27
Category
Article
ISSN
0954-7894

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Clinical phenotype and mutations in conn
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✍ Cohn, Edward S.; Kelley, Philip M. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 45 KB πŸ‘ 2 views

Mutations in the gene for connexin 26, GJB2, are the most common cause of hearing loss in American and European populations, with a carrier rate of about 3%-a rate similar to that for cystic fibrosis. A single mutation, 35delG, is responsible for most of this autosomal recessive hearing loss, DFNB1.