Documentos relacionados

1. <i>GRN</i> mutation spectrum and genotype-phenotype correlation in Chinese dementia patients: data from PUMCH dementia cohort.
2. Modelling frontotemporal dementia using patient-derived induced pluripotent stem cells.
3. Progranulin in neurodegenerative dementia.
4. Distrofia muscular de cinturas 2J, revisión bibliográfi-ca y reporte de un caso pediátrico en Ecuador
5. Autosomal Dominant Frontotemporal Lobar Degeneration in a Filipino Family with Progranulin Mutation.
6. The molecular basis of frontotemporal dementia.
7. The "New Synthesis".
8. A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review.