Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss.
| Autor: | Elbagoury, Nagham M., Soliman, Hala N., Mohammed, Ola S., Ghorab, Eman A., Elruby, Mona O., El-bassyouni, Hala T., Essawi, Mona L. |
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| Zdroj: | Middle East Journal of Medical Genetics; Jan2014, Vol. 3 Issue 1, p11-15, 5p |
| Databáze: | Complementary Index |
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