Biochemical, biomarker, and behavioral characterization of the GrnR493X mouse model of frontotemporal dementia

DM Smith, G Aggarwal, ML Niehoff, SA Jones… - Molecular …, 2024 - Springer
Heterozygous loss-of-function mutations in the progranulin gene (GRN) are a major cause of
frontotemporal dementia due to progranulin haploinsufficiency; complete deficiency of …
相关文章

Biochemical, biomarker, and behavioral characterization of the GrnR493X mouse model of frontotemporal dementia.

DM Smith, G Aggarwal, ML Niehoff… - Biorxiv: the Preprint …, 2023 - europepmc.org
Heterozygous loss-of-function mutations in the progranulin gene (GRN) are a major cause of
frontotemporal dementia due to progranulin haploinsufficiency; complete deficiency of …

Biochemical, biomarker, and behavioral characterization of the GrnR493X mouse model of frontotemporal dementia

DM Smith, G Aggarwal, ML Niehoff, SA Jones… - bioRxiv, 2023 - biorxiv.org
Heterozygous loss-of-function mutations in the progranulin gene (GRN) are a major cause of
frontotemporal dementia due to progranulin haploinsufficiency; complete deficiency of …

Biochemical, biomarker, and behavioral characterization of the GrnR493X mouse model of frontotemporal dementia

DM Smith, G Aggarwal, ML Niehoff… - … : the preprint server …, 2023 - pubmed.ncbi.nlm.nih.gov
Heterozygous loss-of-function mutations in the progranulin gene (GRN) are a major cause of
frontotemporal dementia due to progranulin haploinsufficiency; complete deficiency of …

Biochemical, biomarker, and behavioral characterization of the GrnR493X mouse model of frontotemporal dementia.

DM Smith, G Aggarwal, ML Niehoff… - Biorxiv: the Preprint …, 2023 - europepmc.org
Heterozygous loss-of-function mutations in the progranulin gene (GRN) are a major cause of
frontotemporal dementia due to progranulin haploinsufficiency; complete deficiency of …