Glial Protein Mutations in Alexander Disease

Authors

  • J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-19-3-11

Keywords:

Glial Fibrillary Acidic Protein, Alexander Disease, Juvenile Variety

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.

Published

2005-03-01

Issue

Section

Degenerative Diseases