Pediatric Neurology Briefs
Published 2010 | Version v1.0.0
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Severe CMD with Novel Mutation in Lamin A/C Gene

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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

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Created
2010
When the item was originally created.