Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects
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| Description | scientific article |
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author: Neil V Morgan Paul Gissen Marie Lordkipanidzé David Allsup Paul Harrison Steve P. Watson Michael Simpson Sian Drake |
| Publication date | June 16, 2016 |
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| Missing/wrong data? | Edit Wikidata item |