Severe CMD with Novel Mutation in Lamin A/C Gene
Researchers at Queen Fabiola Children’s 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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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2010-11-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/731 |