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

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DOIResolve DOI: https://doi.org/10.1016/S1474-4422(07)70221-1
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TypeArticle
Journal titleThe Lancet Neurology
ISSN1474-4422
Volume6
Issue10
Pages857868
Publication date
PublisherElsevier
NRC publication
This is a non-NRC publication

"Non-NRC publications" are publications authored by NRC employees prior to their employment by NRC.

NRC number1773
NPARC number3538364
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Record identifierdbd98829-3d74-4b32-bd93-83405613d6f2
Record created2009-03-01
Record modified2019-07-22
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