A novel deletion in progranulin gene is associated with FTDP-17 and CBS
- 8 December 2006
- journal article
- Published by Elsevier in Neurobiology of Aging
- Vol. 29 (3) , 427-435
- https://doi.org/10.1016/j.neurobiolaging.2006.10.028
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- Novel splicing mutation in the progranulin gene causing familial corticobasal syndromeBrain, 2006
- Characteristics of frontotemporal dementia patients with a Progranulin mutationAnnals of Neurology, 2006
- HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulinAnnals of Neurology, 2006
- The Granulin-Epithelin Precursor Is a Steroid-Regulated Growth Factor in Endometrical CancerReproductive Sciences, 2006
- Phenotypic Variation in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17Dementia and Geriatric Cognitive Disorders, 2004
- From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutationAnnals of Neurology, 1999
- Stimulation of PC Cell-Derived Growth Factor (Epithelin/Granulin Precursor) Expression by Estradiol in Human Breast Cancer CellsBiochemical and Biophysical Research Communications, 1999
- Tau is a candidate gene for chromosome 17 frontotemporal dementiaAnnals of Neurology, 1998
- Faster Linkage Analysis Computations for Pedigrees with Loops or Unused AllelesHuman Heredity, 1996
- Clinical diagnosis of Alzheimer's diseaseNeurology, 1984