Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 - Concepedia

Concepedia

Publication | Closed Access

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

1.5K

Citations

22

References

2006

Year

Marc Cruts, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Hans Wils, Daniel Pirici, Rosa Rademakers, Rik Vandenberghe, Bart Dermaut, Jean‐Jacques Martin,

Neurodegenerative DiseasesAlzheimer's DiseaseMendelian DisorderNull MutationsGenetic DisorderGeneticsDementiaPathologyDegenerative DiseaseFrontotemporal DementiaNeurologyNeurodegenerationMedicineNeurogenetics

References

	Year	Citations

Page 1

Page 1