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Whole-Exome Sequencing Identified CFTR Variants in Two Consanguineous Families in China
BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disease caused by genetic variants of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. It is a common hereditary disease in Caucasians while rare in the Chinese. Until now, only 87 Chinese patients have been reported with...
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| Yayımlandı: | Front Genet |
|---|---|
| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Frontiers Media S.A.
2021
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8283821/ https://ncbi.nlm.nih.gov/pubmed/34276759 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.631221 |
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