Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17

Genomics. 1998 Jul 1;51(1):152-4. doi: 10.1006/geno.1998.5360.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Chromosomes, Human, Pair 17 / genetics*
  • Dementia / complications
  • Dementia / genetics*
  • Exons
  • Frontal Lobe
  • Glial Fibrillary Acidic Protein / genetics*
  • Humans
  • Introns
  • Mutation
  • Parkinson Disease / complications
  • Parkinson Disease / genetics*
  • Polymorphism, Genetic
  • Temporal Lobe

Substances

  • Glial Fibrillary Acidic Protein