Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226)
<p><strong>Objective</strong> To identify novel genetic associations with white matter hyperintensities (WMH).</p> <p><strong>Methods</strong> We performed a genome-wide association meta-analysis of WMH volumes in 11,226 individuals, including 8,429 populati...
| Main Authors: | , , , , , , , , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
American Academy of Neurology
2019
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