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Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients
Genome-wide association studies (GWASs) have identified genes that affect plasma von Willebrand factor (VWF) levels. ABO showed a strong effect, whereas smaller effects were seen for VWF , STXBP5 , STAB2 , SCARA5 , STX2 , TC2N , and CLEC4M . This study screened comprehensively for both common and ra...
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| Publicado en: | TH Open |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Georg Thieme Verlag KG
2020
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7603419/ https://ncbi.nlm.nih.gov/pubmed/33145474 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0040-1718885 |
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