Related Articles
Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery‑Dreifuss muscular dystrophy
Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing
Two novel mutations in ERCC6 cause Cockayne syndrome B in a Chinese family
Clinical diagnosis and genetic counseling of atypical ataxia‑telangiectasia in a Chinese family
Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system