Title : Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment.

Pub. Date : 2021 Mar 25

PMID : 33767277






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 CADASIL is a small vessel disease caused by mutations in NOTCH3 that lead to an odd number of cysteines in the EGF-like repeat domain, causing protein misfolding and aggregation. Cysteine notch receptor 3 Homo sapiens