Clinical Features and Outcome of Hypertrophic ...
request. The screening analysis revealed 36 MYH7,24 MYBPC3,20TTNT2,6TNNI3,2MYL2,1TPM1,1 TTN, and 2 MYL3 mutations in 91 familial HCM cases, and 5 MYBPC3,3TNNT2,3TNNI3,1MYL3,1TTN, and 2 MYH7 mutations in 15 sporadic HCM cases. In addition, we found 1 DES and 3 TTN mutations in four familial DCM cases and 1 TTN and 3 DMD mutations in four sporadic DCM cases (details will be … ................
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