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: | Engle Elizabeth C, O'Brien Kristine F, Kunkel Louis M |
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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 |
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