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Rare large homozygous CFTR gene deletion in an Iranian patient with cystic fibrosis
Cystic fibrosis, a common autosomal recessive genetic disorder among Caucasians, is caused by defects in the transmembrane conductance regulatory (CFTR) gene. The analysis of CFTR gene mutations is useful to better characterize the disease, and for preconceptional screening, prenatal and preimplanta...
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| Asıl Yazarlar: | , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Baishideng Publishing Group Inc
2014
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4133434/ https://ncbi.nlm.nih.gov/pubmed/25133155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v2.i8.395 |
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