Insights into disease mechanisms of cardiomyopathy in the presence of the CSRP3 C58G mutation-MedSci.cn

Insights into disease mechanisms of cardiomyopathy in the presence of the CSRP3 C58G mutation

Ehsan, M; Kelly, M; Hooper, C; Beglov, J; Davies, B; Redwood, C; Watkins, H; Gehmlich, K