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Epidemiological study of nonsyndromic hearing loss in Sicilian newborns

✍ Scribed by M. Niceta; C. Fabiano; P. Sammarco; M. Piccione; V. Antona; M. Giuffrè; G. Corsello


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
88 KB
Volume
143A
Category
Article
ISSN
1552-4825

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✍ DA Scott; ML Kraft; R Carmi; A Ramesh; K Elbedour; Y Yairi; C. R. Srikumari Sris 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 223 KB 👁 1 views

Mutations in the Cx26 gene have been shown to cause autosomal recessive nonsyndromic hearing loss (ARNSHL) at the DFNB1 locus on chromosome 13q12. Using direct sequencing, we screened the Cx26 coding region of affected and nonaffected members from seven ARNSHL families either linked to the DFNB1 loc