Congratulation to Margaret Chan Familial and Sporadic GJB2-Related Deafness in Iran: Review of Gene Mutations
Background: Mutations in the GJB2 gene encoding connexin 26 protein, are the main cause for autosomal recessive and sporadic non syndromic hearing loss in many populations. Here, we have taken together and reviewed results from our six previous publications, our unpublished data from ten Iranian pro...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Liburua |
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Tehran University of Medical Sciences,
2007-03-01T00:00:00Z.
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| Sarrera elektronikoa: | Connect to this object online. |
| Etiketak: |
Etiketa erantsi
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Internet
Connect to this object online.3rd Floor Main Library
| Sailkapena: |
A1234.567 |
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| Alea 1 | Eskuragarri |