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: | Book |
| Published: |
Pediatric Neurology Briefs Publishers,
2010-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |