Multi-exon deletions of the <it>FBN1</it> gene in Marfan syndrome
<p>Abstract</p> <p>Background</p> <p>Mutations in the fibrillin -1 gene <it>(FBN1)</it> cause Marfan syndrome (MFS), an autosomal dominant multi-system connective tissue disorder. The 200 different mutations reported in the 235 kb, 65 exon-containing gene in...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2001-10-01
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| Series: | BMC Medical Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2350/2/11 |