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Clinical and genetic characterization of manifesting carriers of DMD mutations.
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Clinical and genetic characterization of manifesting carriers of DMD mutations.
Clinical and genetic characterization of manifesting carriers of DMD mutations. Neuromuscul Disord. 2010 Aug; 20(8):499-504.
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PubMed
subject areas
Adolescent
Adult
Cardiomyopathy, Dilated
Child
Child, Preschool
DNA Mutational Analysis
Dystrophin
Female
Heart Function Tests
Heterozygote
Humans
Male
Middle Aged
Muscle Weakness
Muscle, Skeletal
Muscular Dystrophy, Duchenne
Mutation
X Chromosome Inactivation
Young Adult
authors with profiles
Kathryn Swoboda, M.D.