共 50 条
- [35] Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome Human Genetics, 2005, 118 : 508 - 514
- [36] Identification of lamin A/C (LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B Journal of Human Genetics, 2002, 47 : 225 - 228
- [40] A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21 European Journal of Human Genetics, 2004, 12 : 1033 - 1040