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Novel Progranulin Mutation Detected in 2 Patients With FTLD
Frontotemporal lobar degeneration (FTLD) with ubiquitin-positive, tau-negative inclusions, and linkage to chromosome 17 was recently found to be caused by mutations in the progranulin (PGRN) gene. In this study, we screened a group of 51 FTLD patients for PGRN mutations and identified a novel exon 6...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2011
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3710288/ https://ncbi.nlm.nih.gov/pubmed/20975516 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WAD.0b013e3181fbc22c |
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