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HEREDITARY SPASTIC PARAPLEGIA (COMPLETE PANEL) , PANEL MASSIVE SEQUENCING (NGS) 80 GENES
| Test Code |
58502 |
|---|---|
| Gene/s |
See all genes  Hide all genes  80 gens |
| Specific Gene |
ABCD1, ADAR, AFG3L2, AIMP1, ALDH18A1, ALS2, AMPD2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, ARG1, ARL6IP1, ARSI, ATL1, ATP13A2, ATP2B4, B4GALNT1, BICD2, BSCL2, c12orf65, C19orf12, CCT5, CYP27A1, CYP2U1, CYP7B1, DDHD1, DDHD2, ENTPD1, ERLIN1, ERLIN2, EXOSC3, FA2H, FARS2, GBA2, GJC2, HACE1, HSPD1, KIF1A, KIF1C, KIF5A, L1CAM, MAG, MARS1, NIPA1, NKX6-2, NT5C2, OPA3, PGAP1, PLP1, PNPLA6, POLR3A, REEP1, REEP2, RNASEH2B, RTN2, SACS, SERAC1, SLC16A2, SLC25A46, SLC2A1, SLC33A1, SPAST, SPG11, SPG20, SPG21, SPG7, TECPR2, TFG, TUBB4A, USP8, VAMP1, VPS37A, WASHC5, WDR45B, WDR48, ZFR, ZFYVE26, ZFYVE27 |
| Analysis Methods |
Massive sequencing data analysis (NGS) |
| Sample Requirements |
10 mL whole blood (EDTA). Necessary clinical and family history. |
| TAT |
30 days |
| Omim G |
– |
| Omim F |
– |
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