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 complex in skeletal and extraoc...
Сохранить в:
| Главные авторы: | , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BMC
2001-02-01
|
| Серии: | BMC Genetics |
| Online-ссылка: | http://www.biomedcentral.com/1471-2156/2/3 |
| Метки: |
Нет меток, Требуется 1-ая метка записи!
|