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Esegui una ricerca nel nostro database

TAT:

Tipo di Campione:

EDTA, LA, VC

Metodica:

NGS

Analisi presente in:

Neurologia, Ortopedia

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Paraparesi Spastica Familiare – Pannello

32 genes: SPG1 (L1CAM), SPG11, SPG4 (SPAST), SPG20, SPG3A (ATL1), SPG17 (BSCL2), SPG9A (ALDH18A1), SPG35 (FA2H), SPG5A(CYP7B1), SPG6 (NIPA1), SPG2 (PLP1), SPG12 (RTN2), SPG31 (REEP1), SPG10 (KIF5A), SPG50 (AP4M1), SPG51 (AP4E1), SPG47 (AP4B1), SPG52 (AP4S1), SPG15 (ZFYVE26), SPG55 (C12orf65), SPG7, SPG30 (KIF1A), SPG64 (ENTPD1), SPG42 (SLC33A1), SPG9B (ALDH18A1), SPG13 (HSPD1), SPG8 (KIAA0196), SPG18 (ERLIN2), SPG33 (ZFYVE27), SPG48 (AP5Z1), SPG43 (C19orf12), SPG39 (PNPLA6)

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Geni/Polimorfismi:

ALDH18A1, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, ATL1, BSCL2, C12ORF65, C19orf12, CYP7B1, ENTPD1, ERLIN2, FA2H, HSPD1, KIAA0196, KIF1A, KIF5A, L1CAM, NIPA1, PLP1, PNPLA6, REEP1, RTN2, SLC33A1, SPAST, SPG11, SPG20, SPG7, ZFYVE26, ZFYVE27

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info@laboratoriogenoma.eu

+39 06164161500

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