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The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID)
Next Generation Sequencing (NGS) has uncovered hundreds of common and rare genetic variants involved in complex and rare diseases including immune deficiencies in both an autosomal recessive and autosomal dominant pattern. These rare variants however, cannot be classified clinically, and common vari...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8050305/ https://www.ncbi.nlm.nih.gov/pubmed/33859323 http://dx.doi.org/10.1038/s41598-021-87898-1 |