Glial Protein Mutations in Alexander Disease

J Gordon Millichap

doi:10.15844/pedneurbriefs-19-3-11

Glial Protein Mutations in Alexander Disease

Pediatric Neurology Briefs

Volume 19 (2005): Issue 3

By: J Gordon Millichap

Open Access

|Mar 2005

Abstract

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.

References

Li R Johnson AB Salomons G Goldman JE Naidu S Quinlan R Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease Ann Neurol 2005 Mar 57 3 310 326 10.1002/ana.20406 15732097
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-19-3-11 | Journal eISSN: 2166-6482

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Language: English

Page range: 24 - 24

Published on: Mar 1, 2005

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Glial Fibrillary Acidic Protein,

Alexander Disease,

Juvenile Variety

© 2005 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 19 (2005): Issue 3