تحميل...
Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations
Mutations in the GJB2 gene are the most common cause of pre-lingual hearing loss (HL) worldwide. Previous studies have shown the frequency of GJB2 mutations to be 16% in Iran, but varies among different ethnic groups. Here, we have reviewed results from previous published mutation reports to provide...
محفوظ في:
| الحاوية / القاعدة: | Intractable Rare Dis Res |
|---|---|
| المؤلفون الرئيسيون: | , , , , |
| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2019
|
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6743427/ https://ncbi.nlm.nih.gov/pubmed/31523594 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2019.01070 |
| الوسوم: |
إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
|