Article
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes.
Neuromuscular disorders : NMD - 1 Jul 1994
Angelini C, Fanin M, Pegoraro E, Freda M P, Cadaldini M, Martinello F
Abstract excerpt
A multidisciplinary study was conducted in order to assess dystrophin expression in a large series of mild X-linked muscular dystrophy patients, with well-defined clinical phenotype. Patients (104) were divided in 4 clinical groups, according to clinical severity: asymptomatic (sub-clinical), ben...
Topics
- Adolescent
- Adult
- Aged
- Blotting, Western
- Child
- Child, Preschool
- Dystrophin
- Genetic Linkage
- Humans
- Immunohistochemistry
- Middle Aged
- Muscular Dystrophies
- Phenotype
- Severity of Illness Index
- X Chromosome