Infantile-Onset Alexander Disease
Abstract
Researchers at the All India Institute of Medical Sciences, New Delhi, India, and VU University Medical Center, Amsterdam report a 6-year-old Indian boy with infantile-onset Alexander disease having an unusually mild clinical course and a de novo mutation in the glial fibrillary acidic protein (GFAP) gene.
DOI: https://doi.org/10.15844/pedneurbriefs-26-7-10 | Journal eISSN: 2166-6482
Language: English
Page range: 56 - 56
Published on: Jul 1, 2012
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2012 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.