Whole-exome sequencing identifies matrisomal gene associations in monogenic cerebral small vessel disease. Guyler SK, Alfayyadh MM, Maksemous N, Lea RA, et al. J Neurol 2026;273:478.

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Amedeo Smart

Independent Medical Education

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Guyler SK, Alfayyadh MM, Maksemous N, Lea RA, et al. Whole-exome sequencing identifies matrisomal gene associations in monogenic cerebral small vessel disease. J Neurol 2026;273:478.
PMID: 42481886