Gliedergürtelmuskeldystrophie (LGMD), Basisdiagnostik

ANO5, CAPN3, CAV3, DYSF, FKRP, FKTN, LMNA, MYOT (TTID), SGCA, SGCB, SGCD, SGCG, TCAP, TRIM32

Gliedergürtelmuskeldystrophie (LGMD) – autosomal dominant

CAV3, DES, DNAJB6, HNRNPDL, LMNA, MYOT, TNPO3

ANK2, CALM1, CASQ2, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, PKP2, RYR2, SCN4B, SNTA1, TRDN

ACTC1, ACTN2, CAV3, CSRP3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, PLN, TCAP, TNNC1, TNNI3, TNNT2, TPM1, VCL

ANK2, CACNA1C, CACNA2D1, CACNB2, CAV3, GPD1L, HCN4, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ5, KCNQ1, PKP2, SCN1B, SCN4B, SCN5A, SNTA1, TRPM4

CACNA1C, CAV3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNQ1, SCN4B, SCN5A, SNTA1