Congenital and Other Myopathies Panel
Test Information
- Titre
-
Congenital and Other Myopathies Panel
- Catégorie
- Neurogenetics
- Sub Category
-
Neuromuscular Disease
- Gene/Platform/Region List
-
ACTA1, ACTN2, ACVR1, ADSS1, ASCC3, ATP2A1, BAG3, BICD2, BIN1, CACNA1H, CACNA1S, CASQ1, CAV3, CCDC78, CFL2, CHKB, CLN3, CNTN1, COL12A1, CRYAB, DES, DNAJB4, DNM2, DOK7, ECEL1, EPG5, FHL1, FKBP14, FLNC, FXR1, GATM, GIPC1, HACD1, HNRNPA1, HNRNPA2B1, HRAS, IGHMBP2, ISCU, KBTBD13, KLHL40, KLHL41, KY, LAMA2, LAMP2, LDB3, LMNA, LMOD3, LRP12, MAP3K20, MB, MCOLN1, MEGF10, MICU1, MSTN, MTM1, MYBPC1, MYBPC3, MYH2, MYH3, MYH7, MYL1, MYL2, MYMK, MYO18B, MYOT, MYPN, NEB, PABPN1, PAX7, PIEZO2, PLEC, PYROXD1, RILPL1, RYR1, RYR3, SCN4A, SELENON, SLC25A4, SPEG, SPTBN4, STAC3, STIM1, SVIL, TNNC2, TNNI2, TNNT1, TNNT3, TNPO3, TPM2, TPM3, TRIM32, TRIM54, TRIM63, TRIP4, TTN, UNC45B, VCP, VMA21
- Test type
- Gene Panel
- Samples Accepted
- Blood, DNA, Dried Blood Spot*
- Indications
- Carrier Cascade Testing, Diagnostics
- Test Methodology
- Sequencing
- Methodology Notes
-
Methodology Notes goes here.
- Disease/Condition
-
Congenital and Other Myopathies
Dernière Mise à Jour: 20 juin 2025
