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Screening for primary immunodeficiency diseases by next‐generation sequencing in early life
OBJECTIVE: We aimed to use next‐generation sequencing (NGS) for the early diagnosis of primary immunodeficiency diseases (PIDs) and define its effects on medical management for an infant cohort in early life. METHODS: A single‐centre study was conducted from November 2015 to April 2018. Infants less...
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| Vydáno v: | Clin Transl Immunology |
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| Hlavní autoři: | , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7231820/ https://ncbi.nlm.nih.gov/pubmed/32431812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cti2.1138 |
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