RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data
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| Description | scientific article |
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author: Inge Jonassen Tomasz Stokowy Paweł Sztromwasser Vidar M Steen |
| Publication date | June 10, 2016 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |