[Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias]. [electronic resource]
Producer: 20031201Description: 775-80 p. digitalISSN:- 0035-3787
- Adolescent
- Adult
- Chromosomes, Human, X -- genetics
- Codon, Terminator -- genetics
- Dystrophin -- genetics
- Exons
- Family
- Female
- Gene Silencing
- Heterozygote
- Humans
- Immunohistochemistry
- Male
- Middle Aged
- Muscle Weakness -- etiology
- Muscle, Skeletal -- pathology
- Muscular Dystrophies -- genetics
- Muscular Dystrophy, Duchenne -- genetics
- Pedigree
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Publication Type: Case Reports; English Abstract; Journal Article
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