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Heterogeneous Spectrum of CFTR Gene Mutations in Korean Patients with Cystic Fibrosis
BACKGROUND: Cystic fibrosis (CF) is one of the most common hereditary disorders among Caucasians. The most common mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene have been well established among Caucasian populations. In Koreans, however, there are very few cases of...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Society for Laboratory Medicine
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3129356/ https://ncbi.nlm.nih.gov/pubmed/21779199 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3343/kjlm.2011.31.3.219 |
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