Functional characterization of a novel CSF1R mutation causing hereditary diffuse leukoencephalopathy with spheroids.

Mol Genet Genomic Med · 2019 · PMC6465730 · PMID 30729751

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

a small trendno p-value reported

Additionally, we found a small trend toward higher expression of CSF1R on both classical and nonclassical monocytes of the HDLS patient (Figure 4 c).

also in 722 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.