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Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a devastating disease that probably involves several genetic loci. Several rare genetic variants and one common single nucleotide polymorphism (SNP) of MUC5B have been associated with the disease. Our aim was to identify additional common variants a...
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3894577/ https://ncbi.nlm.nih.gov/pubmed/24429156 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S2213-2600(13)70045-6 |
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