Diagnóstico genético de patologías del sistema esquelético muscular y nervioso
Miopatías hereditarias. Panel NGS (68 genes): CRYAB, LDB3, BAG3, TPM3, NEB, ACTA1, TPM2, TNNT1, KBTBD13, CFL2, TTN, ISCU, MTM1, GNE, VCP, CLCN1, SCN4A, RYR1, SEPN1, DYSF, MYH7, COL6A1, COL6A2, COL6A3, ATP2A1, MATR3, FLNC, CACNA1S, LAMA2, SYNE1, DMD, POMT1, POMT2, FKTN, FKRP, LARGE, POMGNT1, SGCG, SGCA, SGCB, SGCD, CAPN3, TCAP, TRIM32, ANO5, PLEC, DES, MYOT, LMNA, CAV3, DNAJB6, EMD, FHL1, SYNE1, SYNE2, TMEM43, DPAGT1, AGRN, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE, COLQ, DOK7, GFPT1, MUSK, RAPSN.
CRYAB, LDB3, BAG3, TPM3, NEB, ACTA1, TPM2, TNNT1, KBTBD13, CFL2, TTN, ISCU, MTM1, GNE, VCP, CLCN1, SCN4A, RYR1, SEPN1, DYSF, MYH7, COL6A1, COL6A2, COL6A3, ATP2A1, MATR3, FLNC, CACNA1S, LAMA2, SYNE1, DMD, POMT1, POMT2, FKTN, FKRP, LARGE, POMGNT1, SGCG, SGCA, SGCB, SGCD, CAPN3, TCAP, TRIM32, ANO5, PLEC, DES, MYOT, LMNA, CAV3, DNAJB6, EMD, FHL1, SYNE1, SYNE2, TMEM43, DPAGT1, AGRN, CHAT, CHRNA1, CHRNB1, CHRND, CHRNE, COLQ, DOK7, GFPT1, MUSK, RAPSN
Condiciones de Transporte
Código Prueba ICM
ICM101003
Tipo de Muestra
5 ml sangre total EDTA /Saliva
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