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CORTICAL MALFORMATIONS , PANEL MASSIVE SEQUENCING (NGS) 38 GENES
| Test Code |
53555 |
|---|---|
| Gene/s |
See all genes  Hide all genes  38 gens |
| Specific Gene |
ACTB, ACTG1, ADGRG1, AKT3, ARFGEF2, ARX, ASPM, CASK, COL4A1, DCX, DYNC1H1, FKRP, FKTN, FLNA, FOXG1, GPSM2, KIAA1279, LAMA2, LAMB1, LAMC3, LARGE1, NDE1, OCLN, OPHN1, PAFAH1B1, PIK3CA, PIK3R2, POMGNT1, POMT1, POMT2, RELN, SRPX2, TUBA1A, TUBA8, TUBB2B, TUBB3, VLDLR, WDR62 |
| 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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Do you need more information?
Contact us at
genetics@referencelaboratory.es
Are you a verified customer?
Ordering a test or Service from
us is simple and quick
Check our sample requirements
We have optimized all our processes to accept a wide range of samples, always adapting to each case.