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Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran

✍ Scribed by Bonyadi, Mortaza. J.; Fotouhi, Nikou; Esmaeili, Mohsen


Book ID
121509759
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
258 KB
Volume
78
Category
Article
ISSN
0165-5876

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GJB2: The spectrum of deafness-causing a
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Genetic testing was completed on 1,294 persons with deafness referred to the Molecular Otolaryngology Research Laboratories to establish a diagnosis of DFNB1. Exon 2 of GJB2 was screened for coding sequence allele variants by denaturing high-performance liquid chromatography (DHPLC) complemented by