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 |
|---|---|
| Author | Search for: Johnson, S. C. |
| Format | Text |
| Type | 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 | 2019-07-22 |