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Cardiomyopathy


We offer sequencing of a panel of 46 genes linked to inherited cardiomyopathy, developed by Illumina in collaboration with Dr. Heidi Rehm, Dr. Birgit Funke, and their team at the Laboratory for Molecular Medicine (LMM) and Partners Healthcare Center for Personalized Genetic Medicine (PCPGM), Harvard Medical School.
It enriches, through hybridization-based method, the following genes:
ABCC9, ACTC1, ACTN2, ANKRD1, CASQ2, CAV3, CRYAB, CSRP3, CTF1, DES, DSC2, DSG2, DSP, DTNA, EMD, FHL2, GLA, JUP, LAMA4, LAMP2, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, NEXN, PKP2, PLN, PRKAG2, RBM20, RYR2, SGCD, TAZ, TCAP, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL

If you would like to add few genes to this enrichment panel, just ask us.
We will be happy to satisfy your needs and support you.
For further information please fill out the form or write to info@galseq.com.