Adult-onset Alexander disease among patients of Jewish Syrian descent
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s10048-023-00732-w.pdf
Reference29 articles.
1. Brenner M, Johnson AB, Boespflug-Tanguy O et al (2001) Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet 27:117–120. https://doi.org/10.1038/83679
2. Russo LS, Aron A, Anderson PJ (1976) Alexander’s disease: a report and reappraisal. Neurology 26:607–614. https://doi.org/10.1212/wnl.26.7.607
3. Pridmore CL, Baraitser M, Harding B et al (1993) Alexander’s disease: clues to diagnosis. J Child Neurol 8:134–144. https://doi.org/10.1177/088307389300800205
4. Springer S, Erlewein R, Naegele T et al (2000) Alexander disease–classification revisited and isolation of a neonatal form. Neuropediatrics 31:86–92. https://doi.org/10.1055/s-2000-7479
5. Prust M, Wang J, Morizono H et al (2011) GFAP mutations, age at onset, and clinical subtypes in Alexander disease. Neurology 77:1287–1294. https://doi.org/10.1212/WNL.0b013e3182309f72
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