Analysis of mutable exons of neurofibromatosis Type 1 (NF1) gene in Iranian patients
Background: Neurofibromatosis Type 1 (NF1) is an autosomal dominant disease caused by mutations in a tumor suppressor protein called neurofibromin. The NF1 gene consists of 60 exons and due to the large size of the NF1 gene, variation in mutations and the absence of mutation hotspots is a complex pr...
Kaydedildi:
| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Persa |
| Baskı/Yayın Bilgisi: |
Kashan University of Medical Sciences
2023-05-01
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| Seri Bilgileri: | مجله علوم پزشکی فیض (پیوسته) |
| Konular: | |
| Online Erişim: | http://feyz.kaums.ac.ir/article-1-4646-en.pdf |
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