Analysis of human sarcospan as a candidate gene for CFEOM1
<p>Abstract</p> <p>Background</p> <p>Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12). Sarcospan is a member of the dystrophin associated protein c...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2001-02-01
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| Series: | BMC Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2156/2/3 |