Glial Protein Mutations in Alexander Disease
The role of glial fibrillary acidic protein (GFAP) mutations in Alexander disease was analyzed in 44 patients, including 18 with later onset, at the University of Alabama, Birmingham, AL, and at other centers in the US, UK and Europe.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2005-03-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/1315 |