Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C T (Arg493X) mutation: an international initiative

AuthorSearch for:
AffiliationNRC Institute for Marine Biosciences; National Research Council Canada
Peer reviewedNo
NRC number1773
NPARC number3538364
Export citationExport as RIS
Report a correctionReport a correction
Record identifierdbd98829-3d74-4b32-bd93-83405613d6f2
Record created2009-03-01
Record modified2016-05-09
Bookmark and share
  • Share this page with Facebook (Opens in a new window)
  • Share this page with Twitter (Opens in a new window)
  • Share this page with Google+ (Opens in a new window)
Date modified: