G. Bonne

Phenotypic clustering of lamin A/C mutations in neuromuscular patients

E. Bertini, G. Comi, R. Caldara, 2007, Neurology.

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations

M. Komajda, V. Drouin‐Garraud, P. Charron, 2003, Journal of medical genetics.

Amelioration of desmin network defects by αB-crystallin overexpression confers cardioprotection in a mouse model of dilated cardiomyopathy caused by LMNA gene mutation.

M. Makridakis, Y. Capetanaki, C. Davos, 2018, Journal of molecular and cellular cardiology.

Hereditary Neuromuscular Diseases and Cardiac Involvement

K. Wahbi, A. J. van der Kooi, S. S. V. van Westrum, 2020, Clinical Cardiogenetics.