Modifiers of GRN-associated frontotemporal lobar degeneration

E Wauters, S Van Mossevelde, J Van der Zee… - Trends in molecular …, 2017 - cell.com
Heterozygous loss-of-function (LOF) mutations in the human progranulin gene (GRN) cause
frontotemporal lobar degeneration (FTLD) by a mechanism of haploinsufficiency. Patients …
被引用次数：30 相关文章

Modifiers of GRN-associated frontotemporal lobar degeneration

E Wauters, S Van Mossevelde… - Trends in …, 2017 - repository.uantwerpen.be
Heterozygous loss-of-function (LOF) mutations in the human progranulin gene (GRN) cause
frontotemporal lobar degeneration (FTLD) by a mechanism of haploinsufficiency. Patients …

Modifiers of GRN-Associated Frontotemporal Lobar Degeneration

E Wauters, S Van Mossevelde… - Trends in …, 2017 - pubmed.ncbi.nlm.nih.gov
Heterozygous loss-of-function (LOF) mutations in the human progranulin gene (GRN) cause
frontotemporal lobar degeneration (FTLD) by a mechanism of haploinsufficiency. Patients …

Modifiers of GRN-Associated Frontotemporal Lobar Degeneration

E Wauters, S Van Mossevelde, J Van der Zee… - Trends in Molecular …, 2017 - Elsevier
Heterozygous loss-of-function (LOF) mutations in the human progranulin gene (GRN) cause
frontotemporal lobar degeneration (FTLD) by a mechanism of haploinsufficiency. Patients …

Modifiers of GRN-Associated Frontotemporal Lobar Degeneration

E Wauters, S Van Mossevelde, J Van der Zee… - Trends in Molecular …, 2017 - cell.com
Heterozygous loss-of-function (LOF) mutations in the human progranulin gene (GRN) cause
frontotemporal lobar degeneration (FTLD) by a mechanism of haploinsufficiency. Patients …

Modifiers of GRN-Associated Frontotemporal Lobar Degeneration.

E Wauters, S Van Mossevelde… - Trends in Molecular …, 2017 - europepmc.org
Heterozygous loss-of-function (LOF) mutations in the human progranulin gene (GRN) cause
frontotemporal lobar degeneration (FTLD) by a mechanism of haploinsufficiency. Patients …