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

From National Research Council Canada

AuthorSearch for:
FormatText
TypeArticle
Terms of use
Linkhttp://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6X3F-4PKX5T3-1&_user=5226&_coverDate=10%2F31%2F2007&_alid=735303469&_rdoc=7&_fmt=high&_orig=search&_cdi=7297&_sort=d&_docanchor=&view=c&_ct=62&_acct=C000001258&_version=1&_urlVersion=0&_userid=5226&md5=d5a5f182a2de98d66112a88a8ee48fff
NRC number1773
NPARC number3538364
Export citationExport as RIS
Report a correctionReport a correction
Record identifierdbd98829-3d74-4b32-bd93-83405613d6f2
Record created2009-03-01
Record modified2019-02-14
Date modified: