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COMMON VARIABLE IMMUNODEFICIENCY AND RELATED DISORDERS , PANEL MASSIVE SEQUENCING (NGS) 61 GENES
| Test Code |
44789 |
|---|---|
| Gene/s |
See all genes  Hide all genes  61 gens |
| Specific Gene |
ADA, AICDA, AKT1, ATM, BLNK, BTK, CD19, CD27, CD40, CD40LG, CD79A, CD79B, CD81, CR2, CTLA4, CXCL12, CXCR4, DCLRE1C, GATA2, ICOS, IGHM, IGLL1, IKBKB, IKBKG, IL17A, IL17F, IL21, IL21R, IL2RG, IRF4, LRBA, LRRC8A, MLH1, MS4A1, NCF1, NFKB1, NFKB2, NFKBIA, PDCD1, PIK3CD, PIK3R1, PLCG2, PRKDC, PTPRC, RAG1, RAG2, SH2D1A, STAT1, STAT3, TCF7L1, TFRC, TGFB1, TGFB2, TGFB3, TNFRSF13B, TNFRSF13C, TNFRSF4, TNFSF10, TNFSF13B, UNG, XIAP |
| Analysis Methods |
Massive sequencing data analysis (NGS) |
| Sample Requirements |
5 mL whole blood (EDTA). Necessary clinical and family history. |
| TAT |
30 days |
| Omim G |
– |
| Omim F |
– |
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us is simple and quick
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We have optimized all our processes to accept a wide range of samples, always adapting to each case.