参考文献：附:丁香视野肢带型肌营养不良症

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances（LGMD1B）. Hum Mol Genet , 2000 , 9.A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement .Galbiati F , Razani B , Lisanti MP . Caveolae and caveolin-3 in muscular dystrophy .Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23 .Distal anterior compartment myopathy : a dysferlin mutation causing a new muscular dystrophy phenotype .