A new mutation in GFAP widens the spectrum of Alexander disease

Eur J Hum Genet. 2015 Jan;23(1):1-2. doi: 10.1038/ejhg.2014.99. Epub 2014 Jun 25.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Alexander Disease / diagnosis*
  • Alexander Disease / genetics*
  • Codon, Nonsense*
  • Glial Fibrillary Acidic Protein / genetics*
  • Humans
  • Male
  • Protein Interaction Domains and Motifs / genetics*

Substances

  • Codon, Nonsense
  • Glial Fibrillary Acidic Protein