Published 2010
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Journal Article
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Severe CMD with Novel Mutation in Lamin A/C Gene
- Creators
- Millichap, J. Gordon
Abstract
Researchers at Queen Fabiola Childrens University Hospital, Brussels, Belgium, report a 7-year-old Belgian boy with a 5 months-onset congenital muscular dystrophy and laminopathy caused by a de novo heterozygous LMNA gene mutation.
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- PNB-24-88-a
- Created
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2010When the item was originally created.