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The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

โœ Scribed by T. Sobe; S. Vreugde; H. Shahin; M. Berlin; N. Davis; M. Kanaan; Y. Yaron; A. Orr-Urtreger; M. Frydman; M. Shohat; K.B. Avraham


Book ID
118297438
Publisher
Springer
Year
2000
Tongue
English
Weight
303 KB
Volume
106
Category
Article
ISSN
0340-6717

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Identification of mutations in the conne
โœ DA Scott; ML Kraft; R Carmi; A Ramesh; K Elbedour; Y Yairi; C. R. Srikumari Sris ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 223 KB ๐Ÿ‘ 2 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