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Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania

✍ Scribed by C. Lazăr; R. Popp; A. Trifa; C. Mocanu; G. Mihut; C. Al-Khzouz; E. Tomescu; I. Figan; P. Grigorescu-Sido


Book ID
116565497
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
115 KB
Volume
74
Category
Article
ISSN
0165-5876

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