Co-segregation of LMNA and PMP22 gene mutations in the same family. [electronic resource]
- Neuromuscular disorders : NMD Dec 2005
- 858-62 p. digital
Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
0960-8966
10.1016/j.nmd.2005.08.008 doi
Aged DNA Mutational Analysis--methods Family Health Female Hereditary Sensory and Motor Neuropathy--genetics Humans Lamin Type A--genetics Male Middle Aged Muscle, Skeletal--pathology Muscular Dystrophies, Limb-Girdle--genetics Mutation Myelin Proteins--genetics Neural Conduction--physiology