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CSF1R mutations link POLD and HDLS as a single disease entity
Alexandra M. Nicholson
, Matt C. Baker
, Ni Cole A. Finch
, Nicola J. Rutherford
, Christian Wider
, Neill R. Graff-Radford
,
Peter T. Nelson
, H. Brent Clark
, Zbigniew K. Wszolek
, Dennis W. Dickson
, David S. Knopman
, Rosa Rademakers
Pathology and Lab Medicine
Sanders-Brown Center on Aging (SBCoA)
Neuroscience
Neurosurgery
Research output
:
Contribution to journal
›
Article
›
peer-review
146
Scopus citations
Overview
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Medicine and Dentistry
Receptor
100%
Tumor Spheroid
100%
Colony Stimulating Factor 1
100%
Leukodystrophy
100%
Leukoencephalopathy
100%
Diseases
100%
Disease
10%
In Vitro
10%
Phosphotransferase
10%
Biopsy Technique
10%
Receptor Gene
10%
Autophosphorylation
10%
Neurodegenerative Disorder
10%
Nerve Fiber Degeneration
10%
Myelin
10%
Neuroscience
Leukodystrophy
100%
Leukoencephalopathy
100%
Colony Stimulating Factor 1 Receptor
100%
Kinase
10%
Neurodegenerative Disorder
10%
Myelin
10%
In Vitro
10%
Nerve Fiber Degeneration
10%
Receptor Gene
10%
Biochemistry, Genetics and Molecular Biology
Tumor Spheroid
100%
Colony Stimulating Factor 1 Receptor
100%
Genetics
20%
Wild Type
20%
Tyrosine
10%
Receptor Gene
10%
Nerve Fiber Degeneration
10%
Autophosphorylation
10%
Kinase
10%
Phosphotransferase
10%
Myelin
10%
Immunology and Microbiology
Tumor Spheroid
100%
Colony Stimulating Factor 1 Receptor
100%
Wild Type
20%
White Matter
10%
Receptor Gene
10%
Nerve Fiber Degeneration
10%
Autophosphorylation
10%
Myelin
10%
Tyrosine
10%
In Vitro
10%