Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C T (Arg493X) mutation: an international initiative
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C T (Arg493X) mutation: an international initiative
DOI | Resolve DOI: https://doi.org/10.1016/S1474-4422(07)70221-1 |
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Author | Search for: Johnson, S. C. |
Format | Text, Article |
Journal title | The Lancet Neurology |
ISSN | 1474-4422 |
Volume | 6 |
Issue | 10 |
Pages | 857–868 |
Publication date | 2007-10-01 |
Publisher | Elsevier |
NRC publication | This is a non-NRC publication"Non-NRC publications" are publications authored by NRC employees prior to their employment by NRC. |
NRC number | 1773 |
NPARC number | 3538364 |
Export citation | Export as RIS |
Report a correction | Report a correction |
Record identifier | dbd98829-3d74-4b32-bd93-83405613d6f2 |
Record created | 2009-03-01 |
Record modified | 2020-05-10 |