Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B).

By A. Muchir, G. Bonne, A. Kooi, M. V. Meegen, F. Baas, P. Bolhuis, M. D. Visser, K. Schwartz. Human Molecular Genetics, 2000

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Nuclear lamins: building blocks of nuclear architecture. (2002, background): “Consequently, EDMD, FPLD, DCM, and LGMD may represent different degrees of penetrance of the same disease.”
"Laminopathies": a wide spectrum of human diseases. (2007, background): “Subsequently, mutations in LMNA were shown to cause dilated cardiomyopathy 1A [37] and limb-girdle muscular dystrophy 1B [38], both with autosomal dominant inheritance.”